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Medical condition
polyendocrinopathy enteropathy X-linked syndrome (IPEX syndrome) is a rare autoimmune disease. It is one of the autoimmune polyendocrine syndromes. Most often, IPEX
IPEX_syndrome
Medical condition
LINKED syndrome, or LINKage-specific-deubiquitylation-deficiency-induced embryonic defects syndrome, is a rare X-linked genetic disorder caused by mutations
LINKED_syndrome
Health problem from genome abnormalities
affected than females. Some X-linked dominant conditions, such as Rett syndrome, incontinentia pigmenti type 2, and Aicardi syndrome, are usually fatal in males
Genetic_disorder
X-linked dominant genetic disorder
affected than females. This disorder and finding of fragile X syndrome has an X-linked dominant inheritance. It is typically caused by an expansion of
Fragile_X_syndrome
Medical condition
X-linked syndromes include intellectual disability as part of the presentation. These include: Coffin–Lowry syndrome DDX3X syndrome MASA syndrome MECP2
X-linked intellectual disability
X-linked_intellectual_disability
X-linked recessive genetic condition
body tissues. Hunter syndrome is the only MPS syndrome to exhibit X-linked recessive inheritance. The symptoms of Hunter syndrome are comparable to those
Hunter_syndrome
Rare genetic disorder
Lesch–Nyhan syndrome (LNS) is a rare inherited disorder caused by a deficiency of the enzyme hypoxanthine-guanine phosphoribosyltransferase (HGPRT). This
Lesch–Nyhan_syndrome
Rare genetic disease
Kaveggia EG (1974). "Studies of malformation syndromes of man XXXIII: the FG syndrome. An X-linked recessive syndrome of multiple congenital anomalies and mental
FG_syndrome
Medical condition
Lujan–Fryns syndrome (LFS) is an X-linked genetic disorder that causes mild to moderate intellectual disability and features described as Marfanoid habitus
Lujan–Fryns_syndrome
Human genetic metabolism disorder
Barth syndrome (BTHS) is an ultra-rare, but serious X-linked genetic disorder, caused by pathogenic variants in the TAFAZZIN gene, which leads to an inborn
Barth_syndrome
Medical condition
retardation syndrome (ATRX), also called alpha-thalassemia X-linked intellectual disability syndrome, nondeletion type or ATR-X syndrome, is an X-linked recessive
ATR-X_syndrome
Medical condition
Immunodysregulation polyendocrinopathy enteropathy X-linked syndrome (IPEX syndrome) is X-linked recessive due to mutation of the FOXP3 gene on the X
Autoimmune polyendocrine syndrome
Autoimmune_polyendocrine_syndrome
Impairments primarily associated with cannabis use
conflict with scholastic authorities. Marijuana amotivational syndrome is closely linked to self-efficacy, a psychological concept which encapsulates how
Amotivational_syndrome
Medical condition
genome, Alport syndrome can present itself in many forms. This includes X-linked Alport syndrome (XLAS), autosomal recessive Alport syndrome (ARAS), and
Alport_syndrome
Sex-specific patterns of inheritance
chromosome (autosome). In humans, these are termed X-linked recessive, X-linked dominant and Y-linked. The inheritance and presentation of all three differ
Sex_linkage
Medical condition
McLeod syndrome (/məˈklaʊd/ mə-KLOWD) is an X-linked recessive genetic disorder that may affect the blood, brain, peripheral nerves, muscle, and heart
McLeod_syndrome
Association of several clinically recognizable features
"concurrence". When a syndrome is paired with a definite cause this becomes a disease. In some instances, a syndrome is so closely linked with a pathogenesis
Syndrome
Obsolete diagnostic class of autism
Asperger syndrome (AS), also known as Asperger's syndrome or Asperger's, is a formerly used diagnostic category for a condition characterized by significant
Asperger_syndrome
Metabolic disease
Leigh syndrome (also called Leigh disease and subacute necrotizing encephalomyelopathy) is an inherited neurometabolic disorder that affects the central
Leigh_syndrome
Abnormal hair growth over the body
Hypertrichosis (sometimes known as werewolf syndrome or Ambras syndrome) is an abnormal amount of hair growth over the body. The two distinct types of
Hypertrichosis
Genetic neurological disease
Adrenoleukodystrophy (ALD) is a disease linked to the X chromosome. It is a result of fatty acid buildup caused by failure of peroxisomal fatty acid beta
Adrenoleukodystrophy
Genetic disorder
approximate early estimate. X-linked intellectual disability 102 Intellectual developmental disorder, X-linked, syndrome, Snijders Blok type - a record
DDX3X_syndrome
Genetic disorder
Williams syndrome (WS), also Williams–Beuren syndrome (WBS), is a genetic disorder that affects many parts of the body. Facial features frequently include
Williams_syndrome
Genetic disorder
to Hunter syndrome (MPS II); however, Hunter syndrome is X-linked, while Hurler syndrome is autosomal recessive. Children with Hurler syndrome may appear
Hurler_syndrome
Medical condition
syndrome in keeping with Aldrich's original description in 1954. The WAS-related disorders of X-linked thrombocytopenia (XLT) and X-linked congenital
Wiskott–Aldrich_syndrome
Presence of abundant hair between the eyebrows
disability, X-linked 21, 73, 97, and 106 Intellectual disability, X-linked, syndromic 33 Intellectual disability-brachydactyly-Pierre Robin syndrome Intellectual
Unibrow
Group of genetic connective tissues disorders
Ehlers–Danlos syndromes (EDS) are a group of 13 genetic connective tissue disorders. Symptoms often include loose joints, joint pain, stretchy, velvety
Ehlers–Danlos_syndrome
Hormonal disorder in women
Polyendocrine metabolic ovarian syndrome (PMOS), previously called polycystic ovary syndrome (PCOS), is the most common hormonal disorder in women of reproductive
Polyendocrine metabolic ovarian syndrome
Polyendocrine_metabolic_ovarian_syndrome
Rare X-linked dominant condition
Nance–Horan syndrome, also known as X-linked congenital cataracts and microcornea, X-linked cataract–dental syndrome, cataracts-oto-dental syndrome, cataract–dental
Nance–Horan_syndrome
Medical condition
Rett-like syndromes. Pitt-Hopkins syndrome is clinically similar to Angelman syndrome, Rett syndrome, Mowat–Wilson syndrome, and ATR-X syndrome. As more
Pitt–Hopkins_syndrome
X chromosome monosomy
Turner syndrome (TS), commonly known as 45,X, or 45,X0, is a chromosomal disorder in which cells of females have only one X chromosome instead of two,
Turner_syndrome
Medical condition
Oculocerebrorenal syndrome (also called Lowe syndrome) is a rare X-linked recessive disorder characterized by congenital cataracts, hypotonia, intellectual
Oculocerebrorenal_syndrome
Facial muscle paralysis from birth
also be linked to the development of Möbius syndrome. The use of the drugs misoprostol or thalidomide by women during pregnancy has been linked to the
Moebius_syndrome
Medical condition
Christianson syndrome is an X linked syndrome associated with intellectual disability, microcephaly, seizures, ataxia and absent speech. Onset of symptoms
Christianson_syndrome
Medical condition
Aarskog–Scott syndrome (AAS) is a rare disease inherited as X-linked and characterized by short stature, facial abnormalities, skeletal and genital anomalies
Aarskog–Scott_syndrome
Mode of inheritance
the other. Decades of research has shown that the notions "X-linked dominant" and "X-linked recessive" oversimplify the situation and it has been recommended
X-linked recessive inheritance
X-linked_recessive_inheritance
Recessive genetic disorder causing deafblindness
syndrome, also known as Hallgren syndrome, Usher–Hallgren syndrome, retinitis pigmentosa–dysacusis syndrome or dystrophia retinae dysacusis syndrome,
Usher_syndrome
Mode of inheritance
X-linked dominant inheritance, sometimes referred to as X-linked dominance, is a mode of genetic inheritance by which a dominant gene is carried on the
X-linked_dominant_inheritance
Genetic disorder
Down syndrome or Down's syndrome, also known as trisomy 21, is a genetic disorder caused by the presence of all or part of a third copy of chromosome
Down_syndrome
Genetic condition involving facial, heart, blood and skeletal features
Noonan syndrome (NS) is a genetic disorder that may present with mildly unusual facial features, short height, congenital heart disease, bleeding problems
Noonan_syndrome
Autosomal recessive genetic disorder
coordination. Joubert syndrome is one of the many genetic syndromes associated with syndromic retinitis pigmentosa. The syndrome was first identified in
Joubert_syndrome
Medical condition
into the CNS, disease was not rescued. SBMA is a hereditary syndrome, inherited in an X-linked recessive manner. It is transmitted to offspring through the
Spinal and bulbar muscular atrophy
Spinal_and_bulbar_muscular_atrophy
Human genetic disorder
Proteus syndrome is a rare genetic disorder that can cause tissue overgrowth involving all three embryonic lineages. Patients with Proteus syndrome tend
Proteus_syndrome
Medical condition
Blue diaper syndrome is a rare, autosomal recessive or X-linked recessive metabolic disorder characterized in infants by bluish urine-stained diapers
Blue_diaper_syndrome
Medical condition
Wilson-Turner syndrome (WTS), also known as mental retardation X linked syndromic 6 (MRXS6), and mental retardation X linked with gynecomastia and obesity
Wilson–Turner_syndrome
Medical condition
move certain muscles of the eyes, face and tongue. Wieacker syndrome is inherited as an X-linked recessive trait. The condition is characterized by contracture
Wieacker_syndrome
Medical condition
conditions that are linked to higher risk of contracting the condition. Green nail syndrome (chloronychia or Goldman-Fox syndrome) is characterised by
Green_nail_syndrome
X-linked recessive disorder characterised by impulsive behaviour
Brunner syndrome is a rare genetic disorder associated with a mutation in the MAOA gene. It is characterized by lower than average IQ (typically about
Brunner_syndrome
Medical condition
Tranebjaerg–Svejgaard syndrome, also known as X-linked intellectual disability associated with psoriasis is a very rare genetic disorder which is characterized
Tranebjaerg–Svejgaard syndrome
Tranebjaerg–Svejgaard_syndrome
Congenital disorder
The syndrome is inherited in an X-linked recessive manner. Females that possess one copy of the mutation are considered to be carriers of the syndrome but
Simpson–Golabi–Behmel syndrome
Simpson–Golabi–Behmel_syndrome
Neurodevelopmental disorder involving motor and vocal tics
Tourette syndrome (TS), or simply Tourette's, is a motor disorder that begins in childhood or adolescence. It is characterized by multiple movement (motor)
Tourette_syndrome
Psychological phenomenon
researchers have proposed the autism-linked trait of obsessiveness as a contributing factor to savant syndrome. In other words, some savants may over-rehearse
Savant_syndrome
Rare X-linked form of chondrodysplasia punctata
evidence suggests that Conradi–Hünermann syndrome predominantly occurs in females and is usually inherited as an X-linked dominant trait, rare cases in which
Conradi–Hünermann_syndrome
Breakdown of immune system processes
system dysfunction, as seen in IPEX syndrome leads to immune dysfunction, polyendocrinopathy, enteropathy, X-linked (IPEX). IPEX typically presents during
Immune_dysregulation
Malformation of the chest muscle and fingers on one side of the body
Poland syndrome is a birth defect characterized by an underdeveloped chest muscle and short webbed fingers on one side of the body. There may also be short
Poland_syndrome
Condition in which the jaw is small
Intellectual disability, X-linked 61 Intellectual disability, X-linked syndromic, Turner type Intellectual disability, X-linked, syndromic, Bain type Isolated
Micrognathism
Visual impairment
visual disturbances, regardless of lighting conditions. Visual snow syndrome is linked to heightened neural sensitivity in the visual regions of the brain
Visual_snow_syndrome
Medical condition
L1 syndrome is a group of mild to severe X-linked recessive disorders that share a common genetic basis. The spectrum of L1 syndrome disorders includes
L1_syndrome
Genetic disorder involving connective tissue
Marfan syndrome (MFS) is a multi-systemic genetic disorder that affects the connective tissue. People with the condition are often tall and thin, with
Marfan_syndrome
Neuropsychiatric disorder
Alien hand syndrome (AHS) or Dr. Strangelove syndrome is a category of conditions in which a person experiences their limbs acting seemingly on their own
Alien_hand_syndrome
Medical condition
Allan–Herndon–Dudley syndrome (AHDS) is a rare X-linked inherited disorder of brain development that causes both moderate to severe intellectual disability
Allan–Herndon–Dudley_syndrome
Genetic disorder involving an imprinted genomic region
Prader–Willi syndrome (PWS) is a rare genetic disorder caused by a loss of function of specific genes on chromosome 15. In babies, symptoms include weak
Prader–Willi_syndrome
Genetic condition involving hearing loss and depigmentation
Waardenburg syndrome is a group of rare genetic conditions characterised by at least some degree of congenital hearing loss and pigmentation deficiencies
Waardenburg_syndrome
Medical condition
subforms, one with autosomal inheritance and the other X-linked (Xq21.3-q22). The X-linked form is caused by a mutation in a gene CHRDL1 which encodes
Megalocornea
Human chromosomal condition
Klinefelter syndrome (KS), also known as 47,XXY, is a chromosome anomaly. Subjects affected by the condition are almost always phenotypically male (except
Klinefelter_syndrome
Medical condition
recessive, autosomal dominant, x-linked recessive, or mitochondrial inheritance patterns. Oculocerebrofacial syndrome is a very rare autosomal recessive
Blepharophimosis intellectual disability syndromes
Blepharophimosis_intellectual_disability_syndromes
Medical condition
van Den Bosch syndrome is a rare X-linked syndrome like intellectual disability. It may be caused by a small X-chromosome deletion. The condition can be
Van_Den_Bosch_syndrome
Medical condition
MASA syndrome is a rare X-linked recessive neurological disorder on the L1 disorder spectrum belonging in the group of hereditary spastic paraplegias
MASA_syndrome
Medical condition
X-linked dystonia parkinsonism (XDP), also known as lubag syndrome or X-linked dystonia of Panay, is a rare X-linked progressive movement disorder with
X-linked dystonia parkinsonism
X-linked_dystonia_parkinsonism
Symptoms reported by US and Canadian officials abroad
Havana syndrome, also known as anomalous health incidents (AHIs), is a disputed medical condition. Starting in 2016 in about a dozen overseas locations
Havana_syndrome
Autoimmune disease
Sjögren's disease (SjD), previously known as Sjögren syndrome or Sjögren's syndrome (SjS, SS), is a long-term autoimmune disease that primarily affects
Sjögren's_disease
Medical condition
chromosome. Both X-linked Type I and Autosomal dominant Type II Optiz G/BBB syndromes are caused by genetic mutations. However, while the X-linked form is caused
Opitz_G/BBB_syndrome
Medical condition
Occipital horn syndrome (OHS), formerly considered a variant of Ehlers–Danlos syndrome, is an X-linked recessive mitochondrial and connective tissue disorder
Occipital_horn_syndrome
Late day confusion syndrome common among dementia patients
Sundowning, or sundown syndrome, prevalent among people with some form of dementia, is characterized by increased confusion and restlessness beginning
Sundowning
syndrome (WHIM syndrome) Wiskott–Aldrich syndrome X-linked agammaglobulinemia (Bruton syndrome, sex-linked agammaglobulinemia) X-linked hyper-IgM
List_of_skin_conditions
Psychiatric disorder
Capgras delusion or Capgras syndrome (CS) is a psychiatric disorder in which a person holds a delusion that a friend, spouse, parent, other close family
Capgras_delusion
Genetic disorder caused by a mutation of chromosome 15
Angelman syndrome (AS) is a rare genetic disorder that affects approximately 1 in 15,000 individuals. AS impairs the function of the nervous system, producing
Angelman_syndrome
Medical condition
decreased state of consciousness. The syndrome has also been called nonsense syndrome, balderdash syndrome, syndrome of approximate answers, hysterical pseudodementia
Ganser_syndrome
Congenital medical condition
other skeletal malformations as key features. Several reports have linked the syndrome to a mutation in the FBN1 gene, but these cases do not resemble those
Shprintzen–Goldberg_syndrome
Autoimmune disease
Guillain–Barré syndrome (GBS) is a rapid-onset muscle weakness caused by the immune system damaging the peripheral nervous system. Typically, both sides
Guillain–Barré_syndrome
Generalized neurodevelopmental disorder
syndrome. Other genetic conditions include Phelan–McDermid syndrome (22q13del), Mowat–Wilson syndrome, genetic ciliopathy, and Siderius type X-linked
Intellectual_disability
Medical condition
Hoyeraal–Hreidasson syndrome is a very rare multisystem X-linked recessive disorder characterized by excessively short telomeres and is considered a severe
Hoyeraal–Hreidarsson_syndrome
Proposed biological phenomenon
microRNAs. Genes for resistance to parasites might be linked to those for the domestication syndrome; it is predicted that domestic animals are less resistant
Domestication_syndrome
X-linked recessive copper-transport disorder
Menkes disease (MNK), also known as Menkes syndrome, is an X-linked recessive disorder caused by mutations in genes coding for the copper-transport protein
Menkes_disease
Medical condition
Kabuki syndrome (previously known as Kabuki-makeup syndrome (KMS) or Niikawa–Kuroki syndrome) is a rare congenital disorder of genetic origin. It affects
Kabuki_syndrome
Abnormally high heart rate after a postural change
Postural orthostatic tachycardia syndrome (POTS) is a condition characterized by an abnormally large increase in heart rate upon sitting up or standing
Postural orthostatic tachycardia syndrome
Postural_orthostatic_tachycardia_syndrome
Medical condition
Gustavson syndrome, also known as Severe X-linked intellectual disability, Gustavson type, is a rare genetic disorder characterized by severe intellectual
Gustavson_syndrome
Psychiatric behavioural syndrome
Catatonia is a neuropsychiatric syndrome most commonly seen in people with underlying mood disorders such as major depressive disorder, or psychotic disorders
Catatonia
Mental disorder characterized by anger
Intermittent explosive disorder (IED), or episodic dyscontrol syndrome (EDS), is a mental disorder characterized by explosive outbursts of anger or violence
Intermittent explosive disorder
Intermittent_explosive_disorder
Medical condition
corpus callosum agenesis, epilepsy, and spasticity. It is a type of syndromic X-linked intellectual disability. The following list comprises the symptoms
Proud_syndrome
Medical condition
(2019) Renpenning syndrome in a female. Am J Med Genet A RENPENNING H, GERRARD JW, ZALESKI WA, TABATA T (November 1962). "Familial sex-linked mental retardation"
Renpenning's_syndrome
SIDERIUS X-LINKED MENTAL RETARDATION SYNDROME; MRXSSD". omim.org. Retrieved 2019-04-16. "OMIM Entry - # 300705 - CHROMOSOME Xp11.22 DUPLICATION SYNDROME". omim
List_of_genetic_disorders
Genetic brain disorder
Rett syndrome (RTT) is a genetic disorder that typically becomes apparent after 6–18 months of age and almost exclusively in girls. Symptoms include impairments
Rett_syndrome
Nausea and vomiting resulting from cannabis use
Cannabinoid hyperemesis syndrome (CHS) is recurrent nausea, vomiting, and cramping abdominal pain that can occur due to cannabis use. CHS is associated
Cannabinoid hyperemesis syndrome
Cannabinoid_hyperemesis_syndrome
Syndrome resulting from lesions of the medial temporal lobe
Klüver–Bucy syndrome is a syndrome resulting from lesions of the medial temporal lobe, particularly Brodmann area 38, causing compulsive eating, hypersexuality
Klüver–Bucy_syndrome
Genetic disorder
Wu syndrome, also known as X-linked Wu-type intellectual disability, is a rare genetic disorder caused by mutations in the GRIA3 gene located on chromosome
Wu_syndrome
Sudden unexplained death of a child who is less than one year of age
Sudden infant death syndrome (SIDS), sometimes known as cot death or crib death, is the sudden, unexplained death of a child of less than one year of age
SIDS
syntaxin 11 deficiency X-linked lymphoproliferative syndrome Syndromes with autoimmunity: (a) Autoimmune lymphoproliferative syndrome: type 1a (CD95 defects)
List of primary immunodeficiencies
List_of_primary_immunodeficiencies
Medical condition
lives of individuals. It has been linked with depression. Little comprehensive data regarding rumination syndrome in otherwise healthy individuals exists
Rumination_syndrome
Genetic disorder which disrupts normal functioning of the olfactory and pituitary glands
Kallmann syndrome (KS) is a genetic disorder that prevents a person from starting or fully completing puberty. Kallmann syndrome is one of a group of
Kallmann_syndrome
LINKED SYNDROME
LINKED SYNDROME
Boy/Male
British, English
From the Island of Linden Trees
Surname or Lastname
English
English : variant of Lingard.French : occupational name for a maker of or dealer in linen goods, from Old French linge ‘linen (goods)’ (see Linge 1).
Boy/Male
English
Lives by the linden tree.
Girl/Female
English
The linden tree.
Girl/Female
American, Australian, Chinese, Danish, German, Norse, Scandinavian, Swedish
Lime; Linden Tree
Surname or Lastname
Dutch (van Lingen) and German
Dutch (van Lingen) and German : habitational name from Lingen on the Ems river in Lower Saxony, Westphalia, and the former East Prussia.English (Herefordshire) : habitational name from a place in Herefordshire, so named from an old British stream name, Welsh llyn ‘water’ + possibly cain ‘clear’, ‘beautiful’.
Surname or Lastname
English
English : probably a topographic name for someone living in the Lickey Hills, southwest of Birmingham.Perhaps an altered spelling of Scottish Leckie.
Girl/Female
American, Australian, British, Dutch, English, Scottish
A Lake; A Place of Linden Trees
Surname or Lastname
Dutch, German, and Jewish (Ashkenazic)
Dutch, German, and Jewish (Ashkenazic) : variant (plural) of Linde.English : variant spelling of Lindon.Belgian and Dutch (van Linden) : habitational name from places called Linden in Brabant and North Brabant.Dutch (van der Linden) : habitational name from any of numerous places called Ter Linde.Irish : reduced form of McLinden.Swedish (Lindén) : ornamental name from lind ‘lime tree’ + the common suffix -én, from the Latin adjectival ending -enius.
Boy/Male
English
From the linden tree dell.
Female
Yiddish
Pet form of Yiddish Bine, BINKE means "bee."
Female
English
Feminine form of English unisex Lindsay, LINSEY means "Lincoln's wetlands."
Boy/Male
American, Australian, British, English
Valley of the Linden Trees
Female
English
Variant spelling of English Linette, LINNET means "little lake."Â
Boy/Male
American, British, English
Lives by the Linden Tree Hill; From the Island of Linden Trees
Surname or Lastname
Swedish
Swedish : ornamental name from lind ‘lime tree’ + either the German suffix -er denoting an inhabitant, or the surname suffix -ér, derived from the Latin adjectival ending -er(i)us.English (mainly southeastern) : variant of Lind 2.German : habitational name from any of numerous places called Linden or Lindern, named with German Linden ‘lime trees’.
Boy/Male
American, Australian, British, English
From the Linden Tree Hill
Female
Welsh
Old Welsh name derived from the word eilun, LUNED means "idol, image."
Male
English
Variant spelling of English Lyndon, LINDEN means "lime tree hill." Or from the vocabulary word, linden, meaning "lime tree."
Girl/Female
American, Australian, British, Christian, English
Lives by the Linden Tree Hill
LINKED SYNDROME
LINKED SYNDROME
Boy/Male
Indian, Punjabi, Sikh
Novel Warrior
Girl/Female
Latin
An evil nymph.
Girl/Female
Hindu
Goddess Lakshmi, Auspicious, Luster, Prosperity, Pratham, Shrestha
Boy/Male
British, English
Sweet
Female
English
English name derived from the vocabulary word, from Latin delectare, DELIGHT means "to allure, delight."Â
Female
English
 Variant spelling of English Rebekah, REBECKA means "ensnarer." Compare with another form of Rebecka.
Boy/Male
Tamil
Surname or Lastname
English and Scottish
English and Scottish : occupational name meaning ‘servant of Bate’ (see Bate).
Girl/Female
Assamese, Gujarati, Hindu, Indian, Kannada, Malayalam, Marathi, Sindhi, Telugu
Sweet Spoken
Girl/Female
English Greek American Irish
Pure.
LINKED SYNDROME
LINKED SYNDROME
LINKED SYNDROME
LINKED SYNDROME
LINKED SYNDROME
imp. & p. p.
of Kink
n.
The linden. See Linden.
imp. & p. p.
of Link
imp. & p. p.
of Lick
imp. & p. p.
of Ink
a.
Pierced with small holes; worked in eyelets; scalloped on the edge.
n.
The linden tree. See Linden.
imp. & p. p.
of Line
imp. & p. p.
of Wink
a.
Picked out; picked open.
a.
Consisting in real estate or land; as, landed property; landed security.
imp. & p. p.
of Blink
a.
Having limbs; -- much used in composition; as, large-limbed; short-limbed.
n.
Sausages; -- because linked together.
imp. & p. p.
of Pink
a.
Formed by right lines; rectilineal; as, a right-lined angle.
n.
A kind of brick. See Dutch clinker, under Dutch.
a.
With well-proportioned, unblemished limbs; as, a clean-limbed young fellow.
imp. & p. p.
of Clink
imp. & p. p.
of Like