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...

was previously diagnosed with autism, he is now thought to have had FG syndrome. The Utah Film Center's Peek Award honors his legacy. Laurence Kim Peek...

lipomatosis FG syndrome Hallermann–Streiff syndrome Hydrolethalus syndrome Hypomelanosis syndrome Hypomelanosis of Ito Kelvin Peter anomaly plus syndrome Lujan–Fryns...

atrophy-microcephaly-muscle weakness-optic atrophy syndrome Faciocardiorenal syndrome FG syndrome Galloway-Mowat syndrome 4 Gaze palsy, familial horizontal, with...

deletion syndrome 22q11.2 duplication syndrome 22q13 deletion syndrome 2p15-16.1 microdeletion syndrome 2q37 deletion syndrome 3-M syndrome 3C syndrome 3q29...

of Genealogical Societies Fellow of the Geological Society (F.G.S.) FG syndrome Fine guidance sensor Fine Guidance Sensor (HST), FGS for the Hubble Space...

Ehlers–Danlos syndrome Familial dysautonomia (Riley–Day syndrome) FG syndrome Fragile X syndrome GLUT1 deficiency syndrome Griscelli syndrome Type 1 (Elejalde...

Faundes-Banka syndrome Feingold syndrome type 1 FG syndrome 1 Fibrochondrogenesis 2 Fibromuscular dysplasia, multifocal Fontaine progeroid syndrome Frank-Ter...

as part of FG syndrome. Anterior corpus callosum lesions may result in akinetic mutism or anomic aphasia. See also: Alien hand syndrome Dyslexia without...

disorder soon became known as Lujan–Fryns syndrome. Fragile X syndrome Aarskog syndrome Coffin–Lowry syndrome FG syndrome Lacombe, D.; Bonneau, D.; Verloes,...

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...

Lehnhardt FG, Gawronski A, Pfeiffer K, Kockler H, Schilbach L, Vogeley K (November 2013). "The investigation and differential diagnosis of Asperger syndrome in...

regression syndrome, FG syndrome, Johanson–Blizzard syndrome, McKusick–Kaufman syndrome, Pallister–Hall syndrome, short rib–polydactyly syndrome type 1, Townes–Brocks...

syndrome Fetal prostaglandin syndrome Fetal thalidomide syndrome Fetal warfarin syndrome FG syndrome Fiber type disproportion, congenital Fibrinogen deficiency...

Holz FG, Herrmann P (February 2020). "Phenotypic Spectrum of the Foveal Configuration and Foveal Avascular Zone in Patients With Alport Syndrome". Invest...

Kallmann syndrome (KS) is a genetic disorder that prevents a person from starting or fully completing puberty. Kallmann syndrome is a form of a group...

Robinson PN, Symoens S, Van Maldergem L, Debray FG (2014). "Neonatal progeroid variant of Marfan syndrome with congenital lipodystrophy results from mutations...

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...

and hemolytic–uremic syndrome in Argentina". Medicina. 64 (4): 352–6. PMID 15338982. "What is HUS?" (PDF). Corrigan JJ, Boineau FG (November 2001). "Hemolytic–uremic...

Benzodiazepine withdrawal syndrome (BZD withdrawal) is the cluster of signs and symptoms that may emerge when a person who has been taking benzodiazepines...

Robinson PN, Symoens S, Van Maldergem L, Debray FG (2014). "Neonatal progeroid variant of Marfan syndrome with congenital lipodystrophy results from mutations...

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...

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...

; 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...

Wiskott–Aldrich syndrome (WAS) is a rare X-linked recessive disease characterized by eczema, thrombocytopenia (low platelet count), immune deficiency,...

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...

Fetal hemoglobin quantitative trait locus 1; 141749; HBG2 FG syndrome 2; 300321; FLNA FG syndrome 4; 300422; CASK Fibrodysplasia ossificans progressiva;...

(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...

dysfunction syndrome', 'temporomandibular pain dysfunction syndrome', 'temporomandibular joint syndrome', 'temporomandibular dysfunction syndrome', 'temporomandibular...

FG, Jorde LB, Carey JC, Bamshad MJ (2006). "Mutations in embryonic myosin heavy chain (MYH3) cause Freeman-Sheldon syndrome and Sheldon-Hall syndrome"...