AI & ChatGPT searches , social queriess for APERT
Search references for APERT. Phrases containing APERT
See searches and references containing APERT!
Search references for APERT. Phrases containing APERT
See searches and references containing APERT!APERT
Congenital disorder of the skull and digits
Apert syndrome is a form of acrocephalosyndactyly, a congenital disorder characterized by malformations of the skull, face, hands and feet. It is classified
Apert_syndrome
Premature fusion of bones in the skull
Robinow-Sorauf syndrome (now considered a form of Saethre-Chotzen syndrome). Apert syndrome: an abnormal skull shape, small upper jaw, and fusion of the fingers
Craniosynostosis
Abnormally increased distance between two body parts, usually the eyes
DiGeorge syndrome and Loeys–Dietz syndrome. Hypertelorism can also be seen in Apert syndrome, autism spectrum disorder, craniofrontonasal dysplasia, Trisomy
Hypertelorism
Group of diseases
Eugène Apert first to describe a condition characterized by craniosynostosis and syndactyly. The condition described by Apert is now known as the Apert syndrome
Acrocephalosyndactyly
2008 science fiction novel by Neal Stephenson
order would celebrate Apert once every ten years, remaining isolated otherwise. Likewise, a 100-year order would only celebrate Apert every hundred years
Anathem
French pediatrician (1868–1940)
Eugène Charles Apert (27 July 1868 – 2 February 1940) was a French pediatrician born in Paris. He received his doctorate in 1897 and afterwards was associated
Eugène_Apert
Mountain in Rhineland-Palatinate, Germany
Apert is a forested mountain, 631.3 m above sea level (NHN), in the western Volcanic Eifel, a mountain range in the German state of Rhineland-Palatinate
Apert
Medical condition
cell disease, pseudohyperparathyroidism, Turner's syndrome, Down syndrome, Apert syndrome, athyroidism, or osteodystrophy. It most frequently involves the
Brachymetatarsia
Congenital anomaly
may be associated with a high-arched palate include: Allergic rhinitis Apert syndrome Crouzon syndrome Down syndrome Ehlers–Danlos syndrome Friedreich's
High-arched_palate
Condition of fingers or toes being fused together at birth
involved digits. Complex syndactyly occurs as part of a syndrome (such as Apert syndrome) and typically involves more digits than simple syndactyly. Fenestrated
Syndactyly
Abnormal fusion of the radius and ulna bones of the forearm
known genetic syndromes such as Klinefelter syndrome (48,XXXY variant), Apert, Williams, Cornelia de Lange, or Holt–Oram. It has been reported to run
Radioulnar_synostosis
Genetic disorder of the skull and face
were a mother and her daughter, implying a genetic basis.[citation needed] Apert syndrome Treacher Collins syndrome Hearing loss with craniofacial syndromes
Crouzon_syndrome
of a man named Brian Peppers, noted for his appearance, which suggests Apert syndrome or Crouzon syndrome. Found on the Ohio sex offender registry website
List_of_Internet_phenomena
Medical condition
rare conditions, notably: Aarskog–Scott syndrome Acrocallosal syndrome Apert syndrome Bardet–Biedl syndrome CACNA1C-related disorders Carpenter syndrome
Webbed_toes
Abnormally large head size
Signs and Symptoms of Genetic Conditions: A Handbook. Acrocallosal syndrome Apert syndrome Bannayan–Riley–Ruvalcaba syndrome Cardiofaciocutaneous syndrome
Macrocephaly
Protein-coding gene in the species Homo sapiens
cause of several craniosynostosis syndromes: Acrocephalosyndactyly type 1 (Apert syndrome) Beare-Stevenson cutis gyrata syndrome Crouzon syndrome Jackson-Weiss
Fibroblast growth factor receptor 2
Fibroblast_growth_factor_receptor_2
Medical condition
The syndactyly was mitten-like and resembled Apert syndrome but was excluded as being caused by Apert syndrome due to the lack of bony involvement. This
Craniosynostosis, Philadelphia type
Craniosynostosis,_Philadelphia_type
Calcified whitish structure in humans' mouths used to break down food
teeth. Some systemic disorders which may result in hyperdontia include Apert syndrome, cleidocranial dysostosis, Crouzon syndrome, Ehlers–Danlos syndrome
Human_tooth
Russian folklorist
University Press of Mississippi. pp. xxiv, xxvii. ISBN 978-1-62846-094-0. Gruel-Apert 2011. Народные русские легенды [Russian National Legends], Moscow: Direct-Media
Alexander_Afanasyev
Antisense RNA Antisense strand Antisense therapy AP endonuclease AP site Apert syndrome Apoptosis Applied genetics Arg Arrayed library Ascospore Ascus
Index_of_genetics_articles
nonsyndromic cleft patients (Peterson-Falzone et al., 2001). Patients with Apert syndrome have a high occurrence of middle ear disease, otitis media and
Hearing loss with craniofacial syndromes
Hearing_loss_with_craniofacial_syndromes
Anatomical feature of the infant human skull
restriction (IUGR) Premature birth Rarer causes include: Achondroplasia Apert syndrome Cleidocranial dysostosis Congenital rubella Neonatal hypothyroidism
Fontanelle
Medical subspecialty of surgery performed by pediatrics
of conjoined twins Disorders of Sexual Development VACTERL Association Apert Syndrome CHARGE Syndrome Currarino Syndrome Pierre Robin Sequence Prune
Pediatric_surgery
thumbs syndrome Albright's hereditary osteodystrophy Angelman syndrome Apert syndrome (acrocephalosyndactyly) Arthrogryposis–renal dysfunction–cholestasis
List_of_skin_conditions
Diseases named after a person
syndrome (aka Anton syndrome) – Gabriel Anton, Joseph Babinski Apert syndrome – Eugène Apert Aran–Duchenne disease (aka Aran–Duchenne spinal muscular atrophy)
List_of_eponymous_diseases
Skin condition characterized by pimples
risk for acne. Acne can be a feature of rare genetic disorders such as Apert's syndrome. Severe acne may be associated with XYY syndrome. Hormonal activity
Acne
Condition present at birth regardless of cause
paternal age has also been linked to increased risk of achondroplasia and Apert syndrome. Offspring born to fathers under the age of 20 show increased risk
Birth_defect
Title of address for a noble man
Bath's Tale (1388-1396): Loke who that is most vertuous alway Prive and apert, and most entendeth ay To do the gentil dedes that he can And take him for
Gentleman
UBE3A 1:12,000-20,000 Aphalangy-syndactyly-microcephaly syndrome dominant Apert syndrome FGFR2 1:65,000-80,000 Arthrogryposis–renal dysfunction–cholestasis
List_of_genetic_disorders
Syndromes
Anton–Babinski syndrome Aortic arch syndrome Aortocaval compression syndrome Apert syndrome Apparent mineralocorticoid excess syndrome Arakawa's syndrome II
List_of_syndromes
Rules for inflection
nex. verter, sentir -> vers, sens. merger, rumper, avrir -> mers, rupt, apert. g) In other cases, removing the ending gives the desired root. Points a)
De_Wahl's_rule
Earth-goddess in Proto-Indo-European mythology
Labriolle, François de; Sériot, Patrick. "Lise Gruel-Apert, La tradition orale russe (compte-rendu)". In: Revue des études slaves,
Dheghom
- see Cri du chat syndrome Acrania Achondroplasia Acrocephalosyndactyly Apert syndrome Crouzon syndrome Pfeiffer syndrome Acrorenal mandibular syndrome
List_of_congenital_disorders
Hospital in Paris, France
Director Jacques-Joseph Grancher), Director Victor Henri Hutinel, Eugène Apert and Édouard Kirmisson. The entrance of Hôpital des Enfants malades in Rue
Necker–Enfants Malades Hospital
Necker–Enfants_Malades_Hospital
euphemistically referred to as "purging" the French population. Eugène Apert, who served as president of the SFE from 1934, placed immigration at the
Eugenics_in_France
Medical intervention
features commonly include those with craniofacial deformities. Among these, Apert syndrome, Crouzon syndrome, Binder syndrome, Pfeiffer syndrome, and Treacher
Le_Fort_III_osteotomy
Low mountain range in Germany
637 Dockweil Volcanic Eifel 276.81 Limestone Eifel[full citation needed] Apert 631.3 Kyll Volcanic Eifel 276.80 Limestone Eifel Aremberg 623.8 Kempenich
Eifel
a partner of the band showed a CD demo to the then-vocalist of the band Apert Play to Salvador Produções, the company that oversaw Parangolé. Afterwards
Parangolé
Flemish painter (1519–1570)
Jeroen, Frans and Ambrosius, Joos de Beer, Hans de Maier van Herentals, Apert Francen van Delft, Lois van Brussel, Thomas van Coelen, Hans Daelmans van
Frans_Floris
Software for scientific and industrial data visualization and analysis
Development by Modulating Magnitude of Morphological Integration: Evidence from Apert Syndrome Mouse Models". PLOS ONE. 6 (10) e26425. Bibcode:2011PLoSO...626425M
Avizo_(software)
American political adviser (born 1958)
honor their daughter Lili Smith, who died in 2009 from complications due to Apert syndrome, a rare genetic disorder that causes facial and cranial disfiguration
Averell_Smith
Naval defence company based in France
prend le contrôle d'Openhydro". Mer et Marine (in French). 2013. Astrid APERT. "DCNS". Archived from the original on 6 October 2014. Retrieved 27 April
Naval_Group
Albers-Schonberg disease Albright's hereditary osteodystrophy Antley–Bixler syndrome Apert syndrome Beals syndrome Bechterew's Bruck syndrome Camurati–Engelmann disease
List_of_orthopaedic_eponyms
Health effects of an older father at conception
caused by mutations of the FGFR2, FGFR3 and RET genes. These conditions are Apert syndrome, Crouzon syndrome, Pfeiffer syndrome, achondroplasia, thanatophoric
Paternal_age_effect
stenosis Aortic valves stenosis of the child Aortic window Apert like polydactyly syndrome Apert syndrome Aphalangia Aphalangia hemivertebrae Aphalangia
List_of_diseases_(A)
Surgical treatment
fractures, cleft lip and palate, micrognathia, Treacher Collins Syndrome, Apert's Syndrome, Crouzon's Syndrome, Craniofacial microsomia, microtia, and many
Craniofacial_surgery
Medical condition
underdeveloped jaw, beaked nose, hearing loss, and bulging eyes FGFR1 & FGFR2 Apert syndrome Widely spaced eyes, prominent forehead, flat skull posterior, bulging
Saethre–Chotzen_syndrome
Artist Isaac is gay, and hooks up with Ulysses. 2019 Osmosis Netflix Lucas Apert Stéphane Pitti Lucas is gay. He uses Osmosis, a beta dating app, in the
List of dramatic television series with LGBTQ characters: 2016–2019
List_of_dramatic_television_series_with_LGBTQ_characters:_2016–2019
Extraocular muscle that elevates the eye
superior rectus muscle may be congenitally absent. This may be caused by Apert syndrome. This causes a reduced ability to elevate the eye. It may be treated
Superior_rectus_muscle
Transcription factor protein
turricephaly), but also in syndromic forms such as: Acrocephalosyndactyly type 1 (Apert syndrome) (primary FGFR2) Beare-Stevenson cutis gyrata syndrome (primary
Twist-related_protein_1
Species of gastropod
expansum, costa ultima lamelliformi extus munitum. Long., 53; diam., 21; long. apert., 31; lat. intus, 10 mm." This species is found in Alaska at extreme low
Scabrotrophon_stuarti
Medical condition
freckling, neurofibromas, and/or central nervous system (CNS) gliomas. Apert syndrome List of cutaneous conditions Rapini, Ronald P.; Bolognia, Jean
Childhood_tumor_syndrome
French science fiction television series
sister and technical genius creator of Osmosis Stéphane Pitti as Lucas Apert Gaël Kamilindi as Gabriel Suzanne Rault-Balet as Swann Luna Silva as Ana
Osmosis_(TV_series)
Bengali writer
Ahoroni (1957), Anondo Pujabarshiki (1964–69) and Kishore Granthabali. Apert from these works, he also wrote some novels for adults. Nalanda Theke Lumbini
Dhirendralal_Dhar
Musical artist
which he was a member of for a year. He went on to join with his friends Apert Play, all of them without great success. However, with this last band, his
Leo_Santana_(singer)
Human chromosome
containing 1 The following diseases are related to genes on chromosome 10: Apert syndrome Barakat syndrome Beare–Stevenson cutis gyrata syndrome Charcot–Marie–Tooth
Chromosome_10
British geneticist and academic
between paternal age and neurodevelopment disorders. These disorders include Apert syndrome, Achondroplasia, Noonan syndrome and Costello syndrome. Goriely
Anne_Goriely
Slavic mother goddess
Labriolle, François de; Sériot, Patrick. "Lise Gruel-Apert, La tradition orale russe (compte-rendu)". In: Revue des études slaves,
Mat_Zemlya
Growth factor and signaling protein otherwise known as FGF2
CRYSTAL STRUCTURE OF SER252TRP APERT MUTANT FGF RECEPTOR 2 (FGFR2) IN COMPLEX WITH FGF2 1iil: CRYSTAL STRUCTURE OF PRO253ARG APERT MUTANT FGF RECEPTOR 2 (FGFR2)
Fibroblast_growth_factor_2
with. Anwar Chaneil Kular Sex Education Anwar is Nick's boyfriend. Lucas Apert Stéphane Pitti Osmosis Lucas is a user of Osmosis, a beta dating app, that
List of gay characters in television
List_of_gay_characters_in_television
Dutch Golden Age painter
of Delft, the son of Asper Fransz van der Hoeve or Houve, also known as Apert Fransen, who according to Karel van Mander had been a pupil of Frans Floris
Abraham_van_der_Hoef
French general
1894 in Asnières-sur-Seine with Julie Bertrand, divorced wife of Charles Apert. He died on 6 January 1932 in Menton. Frey was a student of the Lycée Thiers
Henri-Nicolas_Frey
- Anterior cruciate ligament reconstruction - Antley–Bixler syndrome - Apert syndrome - Apley grind test - Apley scratch test - Apprehension test - Arachnodactyly
Index of trauma and orthopaedics articles
Index_of_trauma_and_orthopaedics_articles
Study of the image of a horse as a symbol
201 p. (ISBN 9782268059969) (fr) Alexandre Afanassiev (trans. Lise Gruel-Apert), Contes populaires russes, Maisonneuve et Larose, 1992 (fr) Richard Bessière
Horse_symbolism
2011 novel by John Dalton
adults from the State Hospital. One of the counsellors is Wyatt Huddy with Apert Syndrome who has been living in a Salvation Army facility, having been rescued
The Inverted Forest (Dalton novel)
The_Inverted_Forest_(Dalton_novel)
French dermatologist
dermatologist. He studied medicine at the University of Paris as a pupil of Eugène Apert and Émile Achard. In 1912 he received his doctorate with the thesis Les
Albert_Touraine
imperfecta Wilson's disease Albright's disease (fibrous dysplasia of bone) Apert syndrome Conradi's syndrome Craniofacial syndromes Facial deformity syndromes
List of systemic diseases with ocular manifestations
List_of_systemic_diseases_with_ocular_manifestations
American geneticist
Wyrobek, Andrew J; Jabs, Ethylin Wang (2003). "The Paternal-Age Effect in Apert Syndrome is Due, in Part, to the Increased Frequency of Mutations in Sperm"
Ethylin_Wang_Jabs
Fens Aachen (GE), Liège (B) Auf dem Gericht 632.8 West Eifel Vulkaneifel Apert 631.3 South Eifel Eifelkreis Bitburg-Prüm Hohe Warte 628.2 North Eifel Ahrweiler
List of mountains and hills of the Eifel
List_of_mountains_and_hills_of_the_Eifel
Congenital disorder where the nasal passage is blocked
such as Crouzon syndrome, Pfeiffer syndrome, Treacher Collins syndrome, Apert syndrome, and Antley-Bixler syndrome. Choanal atresia is caused by problems
Choanal_atresia
• Anthony Hamilton-Smith, 3rd Baron Colwyn • Antoni Cieszyński • Apert syndrome • Apex locator • Aphthous ulcer • Applied kinesiology •
Index of oral health and dental articles
Index_of_oral_health_and_dental_articles
Romanian composer and conductor (1934–2023)
Chevalier of the Ordre des Arts et des Lettres. Alongside French poet Olivier Apert, Țăranu wrote an opera about the Orestes and Oedipus myths, titled Oreste-Oedipe
Cornel_Țăranu
January – Émile-Félix Gautier, geographer (born 1864) 2 February – Eugène Apert, pediatrician (born 1868) 14 March – Paul Lemoine, geologist (born 1878)
1940_in_France
Malformation of the limbs
syndrome Adams–Oliver syndrome Aglossia adactylia Amniotic band syndrome Apert syndrome Autosomal recessive Robinow syndrome Basel–Vanagaite–Sirota syndrome
Congenital_limb_deformities
Species of gastropod
obtusiuscula. Anfr. 6 plano-convexi, ultimo ampliato, longitudinis 1/3 superante. Apert. semiovalis, marginibus simplicibus, columellari sinuoso. breviter superne
Allopeas_recisa
List of medical conditions involving craniosynostosis
brachyturricephaly Characterized by syndactyly of fingers and toes; usually known as Apert syndrome. Acrocephalosyndactyly type IV Oxycephaly Usually known as Goodman
List of conditions with craniosynostosis
List_of_conditions_with_craniosynostosis
shoulder girdle 755.54 Madelung's deformity 755.55 Acrocephalosyndactyly Apert syndrome 755.9 Limb anomaly, unspec. 756 Other congenital musculoskeletal
List of ICD-9 codes 740–759: congenital anomalies
List_of_ICD-9_codes_740–759:_congenital_anomalies
Disability sport classification system
Syndrome, Autism Spectrum Disorders, and people with Fetal Alcohol Syndrome or Apert Syndrome. In a few cases, it also includes people who acquired their disability
Intellectual disability sport classification
Intellectual_disability_sport_classification
Frequency of mutation of genes
ups and downs of mutation frequencies during aging can account for the apert syndrome paternal age effect. PLos Genetics, 5(7), 1-19. http://users.rcn
Mutation_frequency
the sutures of the skull. He identified the gene mutation responsible for Apert syndrome and the molecular pathways underlying this and other craniosynostosis
Andrew_Wilkie_(geneticist)
Festive tradition from Paris
French). Paris: Apert et Vavasseur. pp. 115–117. Lagarde, J (1856). "Le Carnaval" [The Carnival]. Le Caveau [The Cellar] (in French). Paris: Apert et Vavasseur
Parade of the Fat Ox at the Paris Carnival
Parade_of_the_Fat_Ox_at_the_Paris_Carnival
familial thoracic 6; 611788; ACTA2 Aortic valve disease; 109730; NOTCH1 Apert syndrome; 101200; FGFR2 Aphakia, congenital primary; 610256; FOXE3 Aplasia
List_of_OMIM_disorder_codes
patient in order to correct craniofacial abnormalities such as cleft lip, Apert syndrome, Treacher Collins syndrome, Oligodontia, Cherubism, Crouzon syndrome
Craniofacial_regeneration
Brazilian actress and producer
the story of singer Olivia Byington and her son, João, who was born with Apert syndrome. The play includes music by Byington. O Que é Que Ele Tem was the
Louise_Cardoso
Commune in Bourgogne-Franche-Comté, France
Intercommunality Mirebellois et Fontenois Government • Mayor (2020–2026) Georges Apert Area 1 17.38 km2 (6.71 sq mi) Population (2023) 198 • Density 11.4/km2
Saint-Maurice-sur-Vingeanne
syndrome, Down syndrome, autism spectrum disorders, foetal alcohol syndrome, Apert syndrome) Hearing impairment Adaptive abilities athletes may compete in
Cheerleading_in_Australia
Act of the Parliament of England
said Feast of St. Michael shall bring or cause to be brought privily nor apertly, by himself nor by other, into the said Lands of England, Ireland, Wales
Importation_Act_1337
June - Georges Lacombe, sculptor and painter (died 1916) 27 July - Eugène Apert, pediatrician (died 1940) 28 July - André Spire, poet, writer, and Zionist
1868_in_France
Tunisian poet
Olivier; Bekri, Tahar (2000). Marcher sur l'oubli : entretiens avec Olivier Apert; suivi de poèmes et textes. Paris: L'Harmattan. ISBN 9782738491800. OCLC 55026730
Tahar_Bekri
Medical condition
gene, in chromosome X. It is a feature of various rare disorders such as Apert's syndrome, and can occur alongside other isolated congenital hand/foot malformations
Metacarpal_synostosis
APERT
APERT
APERT
Boy/Male
Hindu, Indian, Sanskrit, Tamil, Telugu
King; Way to Right Path; Leader of Good Way
Boy/Male
Tamil
Lord vishnus son
Girl/Female
Arabic, Muslim
Jasmine; Blessed; Pretty
Boy/Male
Anglo, British, English
Place Name; Brook of the Deer; From the Deer Brook
Boy/Male
Australian, Czechoslovakian, Danish, German, Hungarian, Slavic
Sacred Place; Of the River Tiber
Boy/Male
Indian
Courage, Companion of prophet (Saw)
Biblical
enlightening; appearing
Girl/Female
Biblical
Bound, limit.
Girl/Female
Hindu, Indian
Desire or Want
Female
English
English short form of Greek Barbara, BARB means "foreign; strange."
APERT
APERT
APERT
APERT
APERT
v. t.
To draw through an eye or aperture.
n.
A soft mass, especially of some loose, fibrous substance, used for various purposes, as for stopping an aperture, padding a garment, etc.
n.
A narrow and elongated aperture; a cleft; a fissure.
n.
An opening; an open space; a gap, cleft, or chasm; a passage perforated; a hole; as, an aperture in a wall.
v. t.
To let out at a vent, or small aperture; to give passage or outlet to.
n.
Any one of numerous species of small land snails belonging to the genus Vertigo, having an elongated or conical spiral shell and usually teeth in the aperture.
n.
Any one of numerous species of tubicolous annelids of the genus Serpula and allied genera of the family Serpulidae. They secrete a calcareous tube, which is usually irregularly contorted, but is sometimes spirally coiled. The worm has a wreath of plumelike and often bright-colored gills around its head, and usually an operculum to close the aperture of its tube when it retracts.
n.
The diameter of the exposed part of the object glass of a telescope or other optical instrument; as, a telescope of four-inch aperture.
n.
A hole; an aperture.
n.
The act of opening; an opening; an aperture.
n.
A rent or long aperture; a chink; a fissure; a crack.
n.
A small gate or door, especially one forming part of, or placed near, a larger door or gate; a narrow opening or entrance cut in or beside a door or gate, or the door which is used to close such entrance or aperture. Piers Plowman.
n.
Either one of the two apertures in the calamus of a feather.
n.
A smooth triangular area on the inner surface of the bladder, limited by the apertures of the ureters and urethra.
n.
Any spiral marine gastropod belonging to Turritella and allied genera. These mollusks have an elongated, turreted shell, composed of many whorls. They have a rounded aperture, and a horny multispiral operculum.
n.
A lid, plug, or cover, applied to an aperture so that by its movement, as by swinging, lifting and falling, sliding, turning, or the like, it will open or close the aperture to permit or prevent passage, as of a fluid.
n.
The closing of an aperture in the air passage, or pressure of the finger upon the string, of an instrument of music, so as to modify the tone; hence, any contrivance by which the sounds of a musical instrument are regulated.
n.
A small aperture; a hole or passage for air or any fluid to escape; as, the vent of a cask; the vent of a mold; a volcanic vent.
n.
A small bottle, usually of glass; a little glass vessel with a narrow aperture intended to be closed with a stopper; as, a vial of medicine.
n.
An aperture in a tromp.