Hallermann–Streiff syndrome is a congenital disorder that affects growth, cranial development, hair-growth, and dental development. There are fewer than...
7 KB (627 words) - 15:58, 9 April 2024
Progeria (redirect from Hutchinson Gilford Progeria Syndrome)
lipodystrophy) Cockayne syndrome Ehlers-Danlos syndrome, progeroid form Gerodermia osteodysplastica Hallermann-Streiff syndrome Mandibuloacral dysplasia...
59 KB (6,094 words) - 15:22, 31 May 2024
Adolphus at the battle of Lützen 1632. Hallermann-Streiff syndrome This page lists people with the surname Streiff. If an internal link intending to refer...
526 bytes (96 words) - 14:59, 26 May 2020
Haglund's syndrome Haim–Munk syndrome Hajdu–Cheney syndrome Halal syndrome Hallermann–Streiff syndrome Hamman's syndrome Hamman-Rich syndrome Hand-foot-genital...
41 KB (4,052 words) - 14:48, 24 May 2024
to increased hematopoiesis; see Extramedullary hematopoiesis) Hallermann-Streiff syndrome Dennis, Mark; Bowen, William Talbot; Cho, Lucy (2012). "Frontal...
3 KB (300 words) - 21:52, 31 May 2024
1983 in Townsville, Queensland. Houbolt was born with the rare Hallermann-Streiff syndrome which affects her bone structure and makes her stand at 144 centimetres...
7 KB (532 words) - 01:16, 23 March 2024
Macrocephaly (redirect from Learman syndrome)
lipomatosis FG syndrome Hallermann–Streiff syndrome Hydrolethalus syndrome Hypomelanosis syndrome Hypomelanosis of Ito Kelvin Peter anomaly plus syndrome Lujan–Fryns...
18 KB (1,722 words) - 07:10, 15 April 2024
Ehlers–Danlos syndrome Type III, Ellis–van Creveld syndrome, Gardner's syndrome, Goldenhar syndrome, Hallermann–Streiff syndrome, Orofaciodigital syndrome type...
21 KB (2,484 words) - 20:41, 13 April 2024
Gomez-Lopez-Hernandez syndrome Hallermann-Streiff syndrome Hereditary spastic paraplegia Hirsutism-skeletal dysplasia-intellectual disability syndrome Holoprosencephaly...
14 KB (1,403 words) - 17:30, 15 January 2024
be associated with: Ellis–van Creveld syndrome Hallermann–Streiff syndrome Pierre Robin syndrome Sotos syndrome No intervention is usually recommended...
8 KB (674 words) - 05:47, 25 March 2024
syndrome Gordon syndrome Granulocytopenia with immunoglobulin abnormality Greenberg dysplasia Hajdu-Cheney syndrome Hallermann-Streiff syndrome Hamartoma of...
14 KB (1,343 words) - 23:07, 26 April 2024
are a component of a more extensive syndrome or disease (e.g., cataract resulting from congenital rubella syndrome), one-third occur as an isolated inherited...
10 KB (1,095 words) - 20:59, 30 May 2024
tongue Hajdu–Cheney syndrome Halal–Setton–Wang syndrome Halal syndrome Hall–Riggs mental retardation syndrome Hallermann–Streiff syndrome Hallervorden–Spatz...
21 KB (1,717 words) - 04:04, 12 March 2024
Wilhelm Hallermann, German forensic physician who, along with Enrico Streiff, became the first scientist to identify the Hallermann–Streiff syndrome; in Arnsberg...
85 KB (11,323 words) - 16:04, 22 May 2024
Syndromic microphthalmia is a class of rare congenital anomalies characterized by microphthalmia along with other non-ocular malformations. Syndromic...
13 KB (538 words) - 09:46, 18 March 2024
suggested a diagnosis of either Werner syndrome, Seckel syndrome, Hallermann-Streiff syndrome, or Noonan syndrome. However, the authors thought there were...
4 KB (313 words) - 02:33, 27 September 2023
lip: Macrocheilia Microcheilia chin: Microgenia multiple/other: Hallermann–Streiff syndrome Branchial cleft cyst Neck Webbed neck Ungrouped Preauricular...
4 KB (248 words) - 17:33, 7 October 2023
craniometaphyseal dysplasia; sudden infant death syndrome, which is linked to cardiac arrhythmia; Hallermann–Streiff syndrome; and heart malformations, such as viscero-atrial...
18 KB (1,930 words) - 04:17, 27 May 2024
disease; 169600; ATP2C1 Haim–Munk syndrome; 245010; CTSC Hallermann–Streiff syndrome; 234100; GJA1 Hand-foot-uterus Syndrome; 140000; HOXA13 Harderoporphyria;...
234 KB (18,877 words) - 15:43, 9 May 2024
dystrophy.) François-Neetens dystrophy Fraser-François syndrome Hallermann–Streiff–François syndrome J. E. WINKELMAN, Award of the Donders Medal to Prof...
5 KB (595 words) - 01:07, 12 January 2023
Dallapiccola, B (2004). "A homozygous GJA1 gene mutation causes a Hallermann-Streiff/ODDD spectrum phenotype". Human Mutation. 23 (3): 286. doi:10.1002/humu...
173 KB (17,264 words) - 08:00, 8 May 2024