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There is a page named "Weill-Marchesani syndrome" on Wikipedia
Weill–Marchesani syndrome is a rare genetic disorder characterized by short stature; an unusually short, broad head (brachycephaly) and other facial abnormalities;...4 KB (323 words) - 09:02, 16 May 2022
Fibrillin-1 (section Marfan syndrome)including fetal death, developmental problems, Marfan syndrome or in some cases Weill-Marchesani syndrome. FBN1 is a 230-kb gene with 65 coding exons that...29 KB (3,706 words) - 11:06, 2 September 2024- Acromicric dysplasia (redirect from Moore Federman syndrome)stiff skin syndrome, Marfan syndrome and its variant Marfanoid–progeroid–lipodystrophy syndrome, autosomal dominant Weill-Marchesani syndrome, isolated...3 KB (232 words) - 21:31, 25 February 2024
- syndrome Watson syndrome Weaver syndrome Weber's syndrome Weill–Marchesani syndrome Weismann-Netter–Stuhl syndrome Weissenbacher–Zweymüller syndrome Wellens'...42 KB (4,068 words) - 22:25, 3 September 2024
- dysplasia, Marfan syndrome and its variant Marfanoid–progeroid–lipodystrophy syndrome, autosomal dominant Weill-Marchesani syndrome, isolated ectopia...3 KB (184 words) - 06:54, 6 November 2023
nose-acral anomalies syndrome Weill-Marchesani syndrome Apert syndrome Carpenter syndrome Microcephaly Pfeiffer syndrome Saethre-Chotzen syndrome In humans, brachycephaly...15 KB (1,463 words) - 10:18, 20 August 2024
number of disorders including Peter's anomaly, Marfan syndrome, and Weill–Marchesani syndrome. The spherical shape is caused by an underdeveloped zonule...3 KB (170 words) - 02:38, 13 January 2024- List of systemic diseases with ocular manifestations (section Chromosomal disorders and genetic syndromes)Hemochromatosis Histiocytosis Homocystinuria Lipidoses Marfan's syndrome Weill–Marchesani syndrome Mucopolysaccharidosis Niemann–Pick disease Osteogenesis imperfecta...10 KB (804 words) - 23:08, 22 August 2024
appears to be a strong familial component. Axenfeld syndrome Peters-plus syndrome Weill–Marchesani syndrome "The glaucomas". Parsons' diseases of the eye (22nd ed...8 KB (829 words) - 11:08, 7 March 2024
lentis: More common: Marfan syndrome (upward and outward) Homocystinuria (downward and inwards) Weill–Marchesani syndrome Sulfite oxidase deficiency Molybdenum...10 KB (983 words) - 20:03, 2 August 2024- Hypertrichosis cubiti (redirect from Hairy elbow syndrome)disorders including the Floating-Harbor syndrome, Wiedemann-Steiner syndrome, and Weill-Marchesani syndrome. For children with sporadic hypertrichosis...8 KB (646 words) - 03:55, 10 May 2024
development. It is also a candidate gene for autosomal recessive Weill-Marchesani syndrome. GRCh38: Ensembl release 89: ENSG00000142303 – Ensembl, May 2017...5 KB (587 words) - 22:20, 29 September 2022
RefSeq, Jul 2008]. Mutations in ADAMTS17 are associated with Weill-Marchesani syndrome. GRCm38: Ensembl release 89: ENSMUSG00000058145 – Ensembl, May...6 KB (727 words) - 02:54, 28 November 2023
with subluxation, aniridia with cataractous subluxated lens, and Weill-Marchesani syndrome with microspherophakia and glaucoma. In dislocated posterior chamber...26 KB (3,220 words) - 19:56, 10 December 2023- syndrome; 613398; DDX11 Watson syndrome; 193520; NF1 Weaver syndrome; 277590; NSD1 Weill–Marchesani syndrome, dominant; 608328; FBN1 Weill–Marchesani...234 KB (18,877 words) - 15:43, 9 May 2024
- has an article on: Weill-Marchesani syndrome Wikipedia Named after ophthalmologists Georges Weill (1866-1952) and Oswald Marchesani (1900-1952), who first