Graham-Little syndrome or Graham Little-Piccardi-Lassueur syndrome is a cutaneous condition characterized by lichen planus-like skin lesions.: 648 It...
7 KB (568 words) - 08:41, 22 August 2024
Gourmand syndrome Gouverneurs syndrome GRACILE syndrome Graham-Little syndrome Gray baby syndrome Gray platelet syndrome Greater trochanteric pain syndrome Green...
42 KB (4,070 words) - 17:09, 1 October 2024
dominant congenital Laryngomalacia Larynx atresia Lassa fever Lassueur–Graham–Little syndrome Late onset dominant cone dystrophy Lateral body wall defect Laterality...
10 KB (900 words) - 15:15, 1 April 2022
a lot. Trimethylaminuria (TMAU), also known as fish odor syndrome or fish malodor syndrome, is a rare metabolic disorder where trimethylamine is released...
47 KB (5,418 words) - 14:41, 16 September 2024
staphylococcal infection, chronic lupus erythematosus, lichen planopilaris, Graham-Little syndrome, folliculitis decalvans, acne keloidalis nuchae, immunobullous disorders...
5 KB (460 words) - 04:43, 27 April 2024
erythematosus, chronic cutaneous lupus erythmatosus, Graham-Little syndrome, and Parry Romberg syndrome Other diseases: hypothyroidism, hyperthyroidism, hypoparathyroidism...
16 KB (1,830 words) - 12:28, 11 December 2023
Down syndrome (United States) or Down's syndrome (United Kingdom and other English-speaking nations), also known as trisomy 21, is a genetic disorder...
148 KB (14,803 words) - 02:05, 25 September 2024
and two copies of the Y chromosome. XXXYY syndrome is exceptionally rare, with only eight recorded cases. Little is known about its presentation, but associated...
19 KB (2,263 words) - 22:16, 29 June 2024
Proteus syndrome is a rare disorder with a genetic background that can cause tissue overgrowth involving all three embryonic lineages. Patients with Proteus...
18 KB (1,927 words) - 14:46, 18 September 2024
Klinefelter syndrome (KS), also known as 47,XXY, is a chromosome anomaly where a male has an extra X chromosome. These complications commonly include infertility...
48 KB (4,862 words) - 19:21, 3 October 2024
CHARGE syndrome (formerly known as CHARGE association) is a rare syndrome caused by a genetic disorder. First described in 1979, the acronym "CHARGE" came...
14 KB (1,581 words) - 01:36, 19 August 2024
(congenital hypertrichosis lanuginosa) Generalized hyperhidrosis Graham-Little syndrome Granulosis rubra nasi Green nails Gustatory hyperhidrosis Hair casts...
198 KB (17,960 words) - 17:11, 27 September 2024
XXXY syndrome is a genetic condition characterized by a sex chromosome aneuploidy, where individuals have two extra X chromosomes. People in most cases...
15 KB (1,918 words) - 17:50, 1 August 2024
encephalomyelitis/chronic fatigue syndrome, rheumatoid arthritis, lupus, migraines, multiple sclerosis, and autism. There is little evidence to support this hypothesis...
5 KB (469 words) - 17:17, 22 August 2024
Asperger syndrome (AS), also known as Asperger's syndrome or Asperger's, is a term formerly used to describe a neurodevelopmental condition characterized...
115 KB (12,219 words) - 13:16, 3 October 2024
Benign fasciculation syndrome (BFS) is characterized by fasciculation (twitching) of voluntary muscles in the body. The twitching can occur in any voluntary...
12 KB (1,215 words) - 07:02, 31 July 2024
Fragile X syndrome (FXS) is a genetic neurodevelopmental disorder characterized by mild-to-moderate intellectual disability. The average IQ in males with...
59 KB (6,781 words) - 23:00, 17 September 2024
Carpal tunnel syndrome (CTS) is a nerve compression syndrome associated with the collected signs and symptoms of compression of the median nerve at the...
82 KB (9,502 words) - 22:05, 30 September 2024
XYY syndrome, also known as Jacobs syndrome, is an aneuploid genetic condition in which a male has an extra Y chromosome. There are usually few symptoms...
88 KB (9,969 words) - 06:14, 3 September 2024
rabies and white-nose syndrome. White-nose syndrome has been a significant cause of mortality since 2006, killing over one million little brown bats by 2011...
62 KB (6,993 words) - 07:29, 29 August 2024
Feingold syndrome (also called oculodigitoesophagoduodenal syndrome) is a rare autosomal dominant hereditary disorder. It is named after Murray Feingold...
4 KB (324 words) - 18:14, 25 March 2024
Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) is a disabling chronic illness. People with ME/CFS experience profound fatigue that does not...
106 KB (11,141 words) - 01:18, 3 October 2024
version of Graham is implied to be on the autism spectrum, but series creator Bryan Fuller has refuted the idea that he has Asperger syndrome, stating instead...
35 KB (4,692 words) - 07:52, 27 May 2024
Polydactyly (redirect from Varadi Papp syndrome)
common syndromes with concomitant polydactyly". "Pictures of Extra Fingers" (in Dutch). Archived from the original on 11 November 2013. Graham TJ, Ress...
62 KB (7,065 words) - 01:43, 28 August 2024
Lipodystrophy (redirect from Hollander Simons syndrome)
Lipodystrophy syndromes are a group of genetic or acquired disorders in which the body is unable to produce and maintain healthy fat tissue. The medical...
14 KB (1,583 words) - 05:49, 23 July 2024
Tetrasomy X (redirect from 48 xxxx syndrome)
65–68. doi:10.2478/v10034-009-0006-8. Visootsak J, Graham JM (24 October 2006). "Klinefelter syndrome and other sex chromosomal aneuploidies". Orphanet...
40 KB (4,818 words) - 17:50, 1 August 2024
Pentasomy X (redirect from 49 xxxxx syndrome)
1002/ddrr.86. PMC 2996824. PMID 20014372. Visootsak J, Graham JM (24 October 2006). "Klinefelter syndrome and other sex chromosomal aneuploidies". Orphanet...
29 KB (3,393 words) - 17:51, 1 August 2024
Okamoto syndrome (OS), also known as Au–Kline syndrome (AKS), is a very rare autosomal dominant genetic condition characterised by congenital hydronephrosis...
19 KB (1,896 words) - 14:00, 27 October 2023
Cognitive disengagement syndrome (CDS) is a syndrome characterized by developmentally-inappropriate, impairing and persistent levels of decoupled attentional...
55 KB (6,360 words) - 19:29, 2 October 2024
Androgen insensitivity syndrome (AIS) is a condition involving the inability to respond to androgens, typically due to androgen receptor dysfunction. It...
128 KB (12,638 words) - 22:10, 6 September 2024