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Search references for FG SYNDROME. Phrases containing FG SYNDROME
See searches and references containing FG SYNDROME!FG SYNDROME
Rare genetic disease
FG syndrome (FGS) is a rare genetic syndrome caused by one or more recessive genes located on the X chromosome and causing physical anomalies and developmental
FG_syndrome
American savant (1951–2009)
was previously diagnosed with autism, he is now thought to have had FG syndrome. Laurence Kim Peek was born in Salt Lake City, Utah, to Francis "Fran"
Kim_Peek
Syndromes
deletion syndrome 22q11.2 duplication syndrome 22q13 deletion syndrome 2p15-16.1 microdeletion syndrome 2q37 deletion syndrome 3-M syndrome 3C syndrome 3q29
List_of_syndromes
Abnormally large head size
lipomatosis FG syndrome Hallermann–Streiff syndrome Hydrolethalus syndrome Hypomelanosis syndrome Hypomelanosis of Ito Kelvin Peter anomaly plus syndrome Lujan–Fryns
Macrocephaly
State of low muscle tone
Ehlers–Danlos syndrome Familial dysautonomia (Riley–Day syndrome) FG syndrome Fragile X syndrome GLUT1 deficiency syndrome Griscelli syndrome Type 1 (Elejalde
Hypotonia
Medical condition
disorder soon became known as Lujan–Fryns syndrome. Fragile X syndrome Aarskog syndrome Coffin–Lowry syndrome FG syndrome Lacombe, D.; Bonneau, D.; Verloes,
Lujan–Fryns_syndrome
Skull malformation such that one side is flattened
atrophy-microcephaly-muscle weakness-optic atrophy syndrome Faciocardiorenal syndrome FG syndrome Galloway-Mowat syndrome 4 Gaze palsy, familial horizontal, with
Plagiocephaly
White matter tract connecting the two cerebral hemispheres
as part of FG syndrome. Anterior corpus callosum lesions may result in akinetic mutism or anomic aphasia. See also: Alien hand syndrome Dyslexia without
Corpus_callosum
RV, Turner S, Ledbetter DH, Martin CL (1993). "17q12 Recurrent Deletion Syndrome". In Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJ, Stephens K, Amemiya
List_of_genetic_disorders
Topics referred to by the same term
Genealogical Societies Fellow of the Geological Society (F.G.S.) Fergusonite FG syndrome Fine guidance sensor Fine Guidance Sensor (HST), FGS for the Hubble Space
FGS
Obsolete diagnostic class of autism
Lehnhardt FG, Gawronski A, Pfeiffer K, Kockler H, Schilbach L, Vogeley K (November 2013). "The investigation and differential diagnosis of Asperger syndrome in
Asperger_syndrome
Condition in which the jaw is small
Faundes–Banka syndrome Feingold syndrome type 1 FG syndrome 1 Fibrochondrogenesis 2 Fibromuscular dysplasia, multifocal Fontaine progeroid syndrome Frank–Ter
Micrognathism
Birth defect of malformed rectum
regression syndrome, FG syndrome, Johanson–Blizzard syndrome, McKusick–Kaufman syndrome, Pallister–Hall syndrome, short rib–polydactyly syndrome type 1, Townes–Brocks
Imperforate_anus
syndrome Fetal prostaglandin syndrome Fetal thalidomide syndrome Fetal warfarin syndrome FG syndrome Fiber type disproportion, congenital Fibrinogen deficiency
List_of_diseases_(F)
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
Congenital condition where an individual with a 46,XX karyotype is male
Retrieved 2017-11-07. Lisker R, Flores F, Cobo A, Rojas FG (December 1970). "A case of XX male syndrome". Journal of Medical Genetics. 7 (4): 394–398. doi:10
XX_male_syndrome
Medical condition
Holz FG, Herrmann P (February 2020). "Phenotypic Spectrum of the Foveal Configuration and Foveal Avascular Zone in Patients With Alport Syndrome". Invest
Alport_syndrome
Multiprotein complex involved in transcription in eukaryotes
and are prevented by mutations in MED12 that produce the human disease FG syndrome. Thus, the structure of a Mediator complex can be augmented by RNA as
Mediator_(coactivator)
Rare congenital disorder
FG, Jorde LB, Carey JC, Bamshad MJ (2006). "Mutations in embryonic myosin heavy chain (MYH3) cause Freeman-Sheldon syndrome and Sheldon-Hall syndrome"
Freeman–Sheldon_syndrome
Protein-coding gene in humans
hybridization microarray (Array-CGH) defines a new locus (FGS5) for FG syndrome". American Journal of Medical Genetics. Part A. 139 (3): 221–226. doi:10
MID2
Sudden temporary weakening of the heart muscle
Takotsubo cardiomyopathy or takotsubo syndrome (TTS), also known as stress cardiomyopathy, is a type of non-ischemic cardiomyopathy in which there is a
Takotsubo_cardiomyopathy
Fetal hemoglobin quantitative trait locus 1; 141749; HBG2 FG syndrome 2; 300321; FLNA FG syndrome 4; 300422; CASK Fibrodysplasia ossificans progressiva;
List_of_OMIM_disorder_codes
German-American geneticist (1935–2023)
many genetic syndromes, several now known as the "Opitz syndromes" including Smith–Lemli–Opitz syndrome (SLOS), Opitz–Kaveggia syndrome (FGS1), Opitz
John_M._Opitz
Medical condition
Robinson PN, Symoens S, Van Maldergem L, Debray FG (2014). "Neonatal progeroid variant of Marfan syndrome with congenital lipodystrophy results from mutations
Marfanoid–progeroid–lipodystrophy syndrome
Marfanoid–progeroid–lipodystrophy_syndrome
Medical condition
(Odontomatosis) and dysphagia in father and son-a syndromic connection? Z Kinderheilkd 117(2):101-108 Ziebart T, Draenert FG, Galetzka D, Babaryka G, Schmidseder R
Odontoma_dysphagia_syndrome
Disease of blood and kidneys after bacterial infection
PMID 9777854. S2CID 38100845. Corrigan JJ, Boineau FG (November 2001). "Hemolytic–uremic syndrome". Pediatr Rev. 22 (11): 365–9. doi:10.1542/pir.22-11-365
Hemolytic–uremic_syndrome
Medical condition
Benzodiazepine withdrawal syndrome (BZD withdrawal) is the cluster of signs and symptoms that may emerge when a person who has been taking benzodiazepines
Benzodiazepine withdrawal syndrome
Benzodiazepine_withdrawal_syndrome
Protein-coding gene in humans
forms of X-linked dominant Intellectual disability, Lujan-Fryns syndrome and FG syndrome, as well as instances of prostate cancer. Mutations in MED12 are
MED12
Family of proteins that form the nuclear pore complex
role in nuclear import. Some nucleoporins contain FG repeats. Named after phenylalanine and glycine, FG repeats are small hydrophobic segments that break
Nucleoporin
Genetic disorder of sheep
Spider lamb syndrome, also known as spider syndrome and more formally as ovine hereditary chondrodysplasia, is a homozygous recessive disorder affecting
Spider_lamb_syndrome
Disorder involving pauses in breathing during sleep
555–62. doi:10.1016/S0272-5231(21)00394-4. PMID 3910333. Sullivan CE, Issa FG, Berthon-Jones M, Eves L (April 1981). "Reversal of obstructive sleep apnoea
Sleep_apnea
Orphan disease
; Rosado, F.G; Sykes, D.B.; Hoyer, J.D.; Lacy, M.Q. (2015). "Long-term complete clinical and hematological responses of the TEMPI syndrome after autologous
TEMPI_syndrome
Viral disease of birds
vaccines. Smyth JA. "Overview of Egg Drop Syndrome in Poultry". Retrieved 20 February 2019. Van Eck JH, Davellaar FG, Meurelplerman TA, et al. (1976). "Dropped
Egg_drop_syndrome
Range of genetic disorders which cause a person to appear to grow older faster
Robinson PN, Symoens S, Van Maldergem L, Debray FG (2014). "Neonatal progeroid variant of Marfan syndrome with congenital lipodystrophy results from mutations
Progeroid_syndromes
American motivational speaker and YouTuber
Robinson PN, Symoens S, Van Maldergem L, Debray FG (2014). "Neonatal progeroid variant of Marfan syndrome with congenital lipodystrophy results from mutations
Lizzie_Velásquez
Medical condition
PMID 14998933. Debray, FG; Lambert, M; Lortie, A; Vanasse, M; Mitchell, GA (Sep 1, 2007). "Long-term outcome of Leigh syndrome caused by the NARP-T8993C
Neuropathy, ataxia, and retinitis pigmentosa
Neuropathy,_ataxia,_and_retinitis_pigmentosa
Medical condition
hematuria syndrome: case series". W V Med J. 99 (5): 192–3. PMID 14959511. "UpToDate". www.uptodate.com. Hebert LA, Betts JA, Sedmak DD, Cosio FG, Bay WH
Loin_pain_hematuria_syndrome
Infectious disease caused by Borrelia bacteria, spread by ticks
1590/S0100-879X2006005000082. PMID 17401487. Yoshinari NH, Oyafuso LK, Monteiro FG, de Barros PJ, da Cruz FC, Ferreira LG, et al. (1993). "[Lyme disease. Report
Lyme_disease
Ondrey FG, Balog JZ, Rudy SF, McCullagh L, Levy HP, Liberfarb RM, Francomano CA, Griffith AJ (September 2001). "Auditory dysfunction in Stickler syndrome".
Hearing loss with craniofacial syndromes
Hearing_loss_with_craniofacial_syndromes
Maltreatment or neglect of a child
626664. S2CID 145145228. Murphy JM, Jellinek M, Quinn D, Smith G, Poitrast FG, Goshko M (1991). "Substance abuse and serious child mistreatment: prevalence
Child_abuse
Disorders of the muscles and joints connecting the jaw to the skull
dysfunction syndrome', 'temporomandibular pain dysfunction syndrome', 'temporomandibular joint syndrome', 'temporomandibular dysfunction syndrome', 'temporomandibular
Temporomandibular joint dysfunction
Temporomandibular_joint_dysfunction
Life-threatening immune-related blood disease
hemolytic uremic syndrome (aHUS), also known as complement-mediated hemolytic uremic syndrome (not to be confused with hemolytic–uremic syndrome), is an extremely
Atypical hemolytic uremic syndrome
Atypical_hemolytic_uremic_syndrome
Paediatric and children's diseases
ISSN 1469-493X. PMC 8520752. PMID 27211231. Gomella TL, Cunningham MD, Eyal FG, Tuttle DJ (1999). Neonatology: Management, Procedures, On-Call Problems,
Transient tachypnea of the newborn
Transient_tachypnea_of_the_newborn
Medical condition
Wiskott–Aldrich syndrome (WAS) is a rare X-linked recessive disease characterized by eczema, thrombocytopenia (low platelet count), immune deficiency,
Wiskott–Aldrich_syndrome
Genetic disorders
CACNA1C gene: Timothy syndrome, which may or may not occur with syndactyly Short QT syndrome or Brugada syndrome Long QT syndrome or other arrhythmia without
CACNA1C-related_disorders
Substance for treatment of alcoholism
FG-5893 is a chemical from the diphenylbutylpiperazine class of agents. It is a 5-HT1A agonist and a 5-HT2A antagonist. It is believed to be an anxiolytic
FG-5893
Pooling of blood in the veins
peripheral venous insufficiency and should not be confused with post-thrombotic syndrome, a separate condition caused by damage to the deep veins following deep
Chronic_venous_insufficiency
Group of genetic disorders
existing anti-seizure medications. One phenotype is called Temple–Baraitser syndrome (TBS), a very rare autosomal dominant genetic disorder, characterised by
KCNH1-related_disorders
Psychosis beginning suddenly in the first two weeks after childbirth
misidentification syndromes, such as Capgras syndrome (the belief that someone or something familiar has been replaced with an impostor), Fregoli syndrome (the belief
Postpartum_psychosis
Dangerously low blood pressure due to damage from an organ infection
195–205. doi:10.1055/s-0031-1275532. PMID 21506056. S2CID 20763016. Zampieri FG, Bagshaw SM, Semler MW (2023-06-13). "Fluid Therapy for Critically Ill Adults
Septic_shock
Investigational PMS/PMDD drugs
currently under development for clinical use for the treatment of premenstrual syndrome (PMS) or premenstrual dysphoric disorder (PMDD) but are not yet approved
List of investigational PMS/PMDD drugs
List_of_investigational_PMS/PMDD_drugs
Subfamily of viruses in the family Coronaviridae
CS1 maint: DOI inactive as of December 2025 (link) Wang C, Horby PW, Hayden FG, Gao GF (February 2020). "A novel coronavirus outbreak of global health concern"
Coronavirus
Uterine cancer that is located in tissues lining the uterus
Hoffman BL, Schorge JO, Schaffer JI, Halvorson LM, Bradshaw KD, Cunningham FG, eds. (2012). "Endometrial Cancer". Williams Gynecology (2nd ed.). McGraw-Hill
Endometrial_cancer
Precancerous tissue formation in the esophagus
doi:10.1053/j.gastro.2011.04.061. PMC 3152658. PMID 21679712. van Vilsteren FG, Pouw RE, Seewald S, Alvarez Herrero L, Sondermeijer CM, Visser M, Ten Kate
Barrett's_esophagus
Class of antidepressant medication
Alaproclate (GEA-654) Centpropazine Cericlamine (JO-1017) Femoxetine (Malexil; FG-4963) Ifoxetine (CGP-15210) Omiloxetine Panuramine (WY-26002) Pirandamine
Selective serotonin reuptake inhibitor
Selective_serotonin_reuptake_inhibitor
Group of neurological disorders causing seizures
ISBN 978-1-4443-1667-4. Archived from the original on 21 May 2016. Perucca P, Gilliam FG (September 2012). "Adverse effects of antiepileptic drugs". The Lancet. Neurology
Epilepsy
Condition in which damaged skeletal muscle breaks down rapidly
S2CID 7158989. Szczepanik ME, Heled Y, Capacchione J, Campbell W, Deuster P, O'Connor FG (2014). "Exertional rhabdomyolysis: identification and evaluation of the athlete
Rhabdomyolysis
Withdrawal symptoms of opioids
symptoms of withdrawal can include drug craving, anxiety, restless legs syndrome, nausea, vomiting, diarrhea, sweating, and an elevated heart rate. Opioid
Opioid_withdrawal
Medical condition
Keutel syndrome (KS) is a rare autosomal recessive genetic disorder characterized by abnormal diffuse cartilage calcification, hypoplasia of the mid-face
Keutel_syndrome
Antidepressant medication
Psychiatry. 62 (Suppl 15): 12–17. PMID 11444761. Vlaminck JJ, van Vliet IM, Zitman FG (March 2005). "[Withdrawal symptoms of antidepressants]". Nederlands Tijdschrift
Mirtazapine
Medical condition
Holz FG, Herrmann P (February 2020). "Phenotypic Spectrum of the Foveal Configuration and Foveal Avascular Zone in Patients With Alport Syndrome". Invest
Macular_hypoplasia
Drug that reduces appetite
the EMA due to increased risk of heart disease) Butenolide Diethylpropion FG-7142 Phenmetrazine† (withdrawn in some countries due to the danger of addiction)
Anorectic
Common viral infectious disease
Merck Research Laboratories. ISBN 978-0-911910-18-6. Putukian M, O'Connor, FG, Stricker, P, McGrew, C, Hosey, RG, Gordon, SM, Kinderknecht, J, Kriss, V
Infectious_mononucleosis
Benzodiazepine medication
mechanically ventilated, and, along with other treatments, for acute coronary syndrome due to cocaine use. It can be given orally (by mouth), transdermally (on
Lorazepam
Medical condition
search for another cause, such as kidney stones or loin pain-hematuria syndrome. Also, there are no systemic manifestations, so presence of hearing impairment
Thin basement membrane disease
Thin_basement_membrane_disease
Benzodiazepine sedative
including anxiety, seizures, alcohol withdrawal syndrome, muscle spasms, insomnia, and restless legs syndrome. It may also be used to cause memory loss during
Diazepam
syndrome Ulnar–mammary syndrome Van Der Woude syndrome Von Hippel–Lindau syndrome Watson syndrome Werner syndrome (adult progeria) Westerhof syndrome
List_of_skin_conditions
Chest discomfort due to disorder of the heart muscles
1016/S0735-1097(02)01690-X. PMID 11869851. Levine GN, Steinke EE, Bakaeen FG, Bozkurt B, Cheitlin MD, Conti JB, et al. (February 2012). "Sexual activity
Angina
Medical condition
and estrogens) Kallmann syndrome and GnRH insensitivity Valdes-Socin H, Rubio Almanza M, Tomé Fernández-Ladreda M, Debray FG, Bours V, Beckers A. Reproduction
Fertile_eunuch_syndrome
Failure of the brain to process input from one eye
jcrs.2007.07.024. PMID 18053899. S2CID 1886316. Angell LK, Robb RM, Berson FG (December 1981). "Visual prognosis in patients with ruptures in Descemet's
Amblyopia
Genetic disorders of the adrenal gland
December 2024. Retrieved 16 December 2024 – via PR Newswire. Kruse B, Riepe FG, Krone N, Bosinski Ha, Kloehn S, Partsch CJ, et al. (July 2004). "Congenital
Congenital adrenal hyperplasia
Congenital_adrenal_hyperplasia
Peptide hormone
PMID 29480368. El Hayek S, Bitar L, Hamdar LH, Mirza FG, Daoud G (5 April 2016). "Poly Cystic Ovarian Syndrome: An Updated Overview". Frontiers in Physiology
Insulin
American basketball player (born 1993)
enter the NBA in 2014 until he was diagnosed with a mild form of Marfan syndrome. In 2016, he was cleared to continue playing basketball after a two-year
Isaiah_Austin
Benzodiazepine medication
Clonazepam is also effective in the management of acute mania. Restless legs syndrome can be treated using clonazepam as a third-line treatment option, as the
Clonazepam
American biopharmaceutical company
is also developing FG-3180, a PET imaging agent, to help track the cancer and predict responses to FG-3246. A Phase 2 trial of FG-3246 began in September
Kyntra_Bio
Cancer of the skin, integumentary lymph nodes, or other organs
some countries. Sand M, Sand D, Thrandorf C, Paech V, Altmeyer P, Bechara FG (June 2010). "Cutaneous lesions of the nose". Head & Face Medicine. 6 7. doi:10
Kaposi's_sarcoma
Mammalian protein involved in blood clotting
including thrombotic thrombocytopenic purpura, Heyde's syndrome, and possibly hemolytic–uremic syndrome. Increased plasma levels in many cardiovascular, neoplastic
Von_Willebrand_factor
American football player (born 2003)
2025. "Can't-Miss Play: 68-YARD FIELD GOAL! Cam Little delivers longest FG in NFL history". NFL.com. Retrieved November 2, 2025. Baca, Michael (November
Cam_Little
Protein-coding gene in the species Homo sapiens
(monocytic leukemia) 3". Borrow J, Stanton VP, Andresen JM, Becher R, Behm FG, Chaganti RS, Civin CI, Disteche C, Dubé I, Frischauf AM, Horsman D, Mitelman
KAT6A
Hypertension occurring during pregnancy
Health Organization. 2011. hdl:10665/44703. ISBN 978-92-4-454833-2. Cunningham FG, Leveno KJ, Bloom S, Gilstrap L, eds. (2010). Williams obstetrics (23rd ed
Pre-eclampsia
Medical condition
1007/s00415-006-0160-9. PMID 17063320. S2CID 27976718. Mossetti G, Rendina D, Numis FG, Somma P, Postiglione L, Nunziata V (2003). "Biochemical markers of bone turnover
Erdheim–Chester_disease
Flavor enhancer (621 or E621)
headaches and other feelings of discomfort, known as "Chinese restaurant syndrome". Several blinded studies show no such effects when MSG is combined with
Monosodium_glutamate
Antidepressant medication
569–75. doi:10.1016/0006-3223(89)90217-5. PMID 2537663. S2CID 46730665. Boess FG, Martin IL (1994). "Molecular biology of 5-HT receptors". Neuropharmacology
Trazodone
Medical condition
Cardiol. 42 (2): 211–6. doi:10.1016/S0735-1097(03)00579-5. PMID 12875753. Cosio FG, Zager RA, Sharma HM (July 1985). "Atheroembolic renal disease causes hypocomplementaemia"
Cholesterol_embolism
Disease where the kidneys fail to adequately filter waste products from the blood
breakdown, and hemolytic uremic syndrome. Causes of chronic kidney failure include diabetes, high blood pressure, nephrotic syndrome, and polycystic kidney disease
Kidney_failure
SSRI antidepressant
as post-SSRI sexual dysfunction. Serious side effects include serotonin syndrome, mania, seizures, an increased risk of suicidal behavior, and an increased
Fluoxetine
Chemical compound
Services. 50 (6): 13–6. doi:10.3928/02793695-20120508-06. PMID 22589230. Hopkins FG, Cole SW (December 1901). "A contribution to the chemistry of proteids: Part
Tryptophan
Antiplatelet medication
States, 2014 - 2023". ClinCalc. Retrieved 18 August 2025. O'Gara PT, Kushner FG, Ascheim DD, Casey DE, Chung MK, de Lemos JA, et al. (January 2013). "2013
Clopidogrel
or syndromes common to autoimmune disease. Chronic fatigue syndrome Complex regional pain syndrome Eosinophilic esophagitis Gastritis POEMS syndrome Raynaud's
List_of_autoimmune_diseases
Benign tumor made of fat tissue
114–7. doi:10.1007/s00266-002-1492-1. PMID 12016495. S2CID 6701609. Bechara FG, Sand M, Sand D, et al. (2006). "Lipolysis of lipomas in patients with familial
Lipoma
Medical condition
PMID 7550309. S2CID 7779127. Raming K, Gliem M, Issa PC, Birtel J, Herrmann P, Holz FG, Pfau M, Hess K (August 2021). "Visual dysfunction and structural correlates
Sorsby's_fundus_dystrophy
Heart block in the right ventricle
5152/AnatolJCardiol.2021.84375. PMC 8210929. PMID 34100724. S2CID 235368614. Yanowitz FG. "Lesson VI - ECG Conduction Abnormalities". University of Utah School of
Right_bundle_branch_block
Medication used to treat anxiety disorders
concentrating. Serious side effects may include movement disorders, serotonin syndrome, and seizures. Its use in pregnancy appears to be safe but has not been
Buspirone
OTC medication for depression
oxitriptan include appetite loss, nausea, diarrhea, vomiting, and serotonin syndrome. The drug is a centrally permeable monoamine precursor and prodrug of serotonin
Oxitriptan
both as voyp and V-O-I-P. (Main list of acronyms) Top F0–9 FA FB FC FD FE FF FG FH FI FJ FK FL FM FN FO FP FQ FR FS FT FU FV FW FX FY FZ f – (s) Femto F –
List_of_acronyms:_F
Contagious disease caused by SARS-CoV-2
1097/JCMA.0000000000000270. PMC 7153464. PMID 32134861. Wang C, Horby PW, Hayden FG, Gao GF (February 2020). "A novel coronavirus outbreak of global health concern"
COVID-19
Bacterial infection from a cat
(8): 563–70. doi:10.1089/vbz.2013.1512. PMC 4117269. PMID 25072986. Rosado FG, Stratton CW, Mosse CA (2011). "Clinicopathologic correlation of epidemiologic
Cat-scratch_disease
Protein-coding gene in the species Homo sapiens
Coronary Syndromes". The New England Journal of Medicine. 381 (16): 1524–1534. doi:10.1056/NEJMoa1908973. PMID 31475799. O'Gara PT, Kushner FG, Ascheim
P2Y12
Skin condition characterized by pimples
Uğurlucan FG (22 August 2017). "Hirsutism, Acne, and Hair Loss: Management of Hyperandrogenic Cutaneous Manifestations of Polycystic Ovary Syndrome". Gynecology
Acne
Severe confusion that develops quickly, and often fluctuates in intensity
causes, which usually develops over the course of hours to days. As a syndrome, delirium presents with disturbances in attention, awareness, and higher-order
Delirium
FG SYNDROME
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FG SYNDROME