"Hallermann-Streiff syndrome: airway problems during anaesthesia". J Postgrad Med. 40 (4): 216-8. PMID 9136243. "Hallermann- ... Hallermann-Streiff syndrome is a congenital disorder that affects growth, cranial development, hair-growth, and dental ... The genetic cause of Hallermann-Streiff syndrome has not been conclusively determined. It is most likely due to a de novo ... "Hallermann-Streiff syndrome , Genetic and Rare Diseases Information Center (GARD) - an NCATS Program". rarediseases.info.nih. ...
Hallermann-Streiff syndrome; and heart malformations, such as viscero-atrial heterotaxia. There have also been a few cases of ... Mutations in this gene have been associated with ODDD; craniometaphyseal dysplasia; sudden infant death syndrome, which is ... "A homozygous GJA1 gene mutation causes a Hallermann-Streiff/ODDD spectrum phenotype". Human Mutation. 23 (3): 286. doi:10.1002/ ... Connexin Hypoplastic left heart syndrome GRCh38: Ensembl release 89: ENSG00000152661 - Ensembl, May 2017 GRCm38: Ensembl ...
Hallermann-Streiff syndrome This page lists people with the surname Streiff. If an internal link intending to refer to a ...
Hallermann-Streiff syndrome Dennis, Mark; Bowen, William Talbot; Cho, Lucy (2012). "Frontal bossing". Mechanisms of Clinical ... Fragile X syndrome Hurler syndrome Osteopathia Striata with Cranial Sclerosis Pfeiffer syndrome Rubinstein-Taybi syndrome ... Rickets Achondroplasia Acromegaly Basal cell nevus syndrome Congenital syphilis Cleidocranial dysostosis Crouzon syndrome ... Frontal bossing may be seen in a few rare medical syndromes such as acromegaly - a chronic medical disorder in which the ...
Houbolt was born with the rare Hallermann-Streiff syndrome which affects her bone structure and makes her stand at 144 ...
François-Neetens dystrophy Fraser-François syndrome Hallermann-Streiff-François syndrome J. E. WINKELMAN, Award of the Donders ...
... became the first scientist to identify the Hallermann-Streiff syndrome, in Arnsberg, Germany (d. 1975) Died: Sam Browne, 76, ... Wilhelm Hallermann, German forensic physician who, along with Enrico Streiff, ...
Haim-Munk syndrome Hajdu-Cheney syndrome Halal syndrome Hallermann-Streiff syndrome Hamman's syndrome Hamman-Rich syndrome Hand ... syndrome Wende-Bauckus syndrome Werner syndrome Wernicke-Korsakoff syndrome West syndrome Westerhof syndrome Wet lung syndrome ... syndrome Shone's syndrome Short anagen syndrome Short bowel syndrome short limb syndrome Short man syndrome Short QT syndrome ... syndrome Radial tunnel syndrome Rage syndrome Raghib syndrome Raine syndrome Ramos-Arroyo syndrome Ramsay Hunt syndrome type 1 ...
... syndrome Cri du chat syndrome DiGeorge syndrome Ehlers-Danlos syndrome Fetal alcohol syndrome Hallermann-Streiff syndrome ... Patau syndrome) Trisomy 18 (Edwards syndrome) Trisomy 21 (Down syndrome) Wolf-Hirschhorn syndrome X0 syndrome (Turner syndrome ... arthritis Loeys-Dietz syndrome Marfan syndrome Möbius syndrome Noonan syndrome Pierre Robin syndrome Prader-Willi syndrome ... Progeria Silver-Russell syndrome Seckel syndrome Smith-Lemli-Opitz syndrome Stickler syndrome Treacher Collins syndrome Trisomy ...
Ellis-van Creveld syndrome Hallermann-Streiff syndrome Pierre Robin syndrome Sotos syndrome No intervention is usually ... "Ellis-van Creveld syndrome". MedlinePlus : U.S. National Library of Medicine. Retrieved 7 April 2013. Martinez, CR (March 1978 ...
Ellis-van Creveld syndrome, Gardner's syndrome, Goldenhar syndrome, Hallermann-Streiff syndrome, Orofaciodigital syndrome type ... I, Incontinentia pigmenti, Marfan syndrome, Nance-Horan syndrome, and Tricho-rhino-phalangeal syndrome Type 1. Supernumerary ... "Gardner syndrome - About the Disease - Genetic and Rare Diseases Information Center". rarediseases.info.nih.gov. Retrieved 2022 ... However, this approximation varies in terms of location, other associating syndromes that may be present, and the ethnicity of ...
Seckel syndrome, Hallermann-Streiff syndrome, or Noonan syndrome. However, the authors thought there were differences that ... some of the symptoms suggested a diagnosis of either Werner syndrome, ... distinguished this particular case from any other syndrome, suggesting it to be separated into an entity of its own (which it ...
... syndrome Halal-Setton-Wang syndrome Halal syndrome Hall-Riggs mental retardation syndrome Hallermann-Streiff syndrome ... Mcdonald syndrome Hunter-Jurenka-Thompson syndrome Hunter-Macpherson syndrome Hunter-Mcalpine syndrome Hunter-Mcdonald syndrome ... child Heavy metal poisoning HEC syndrome Hecht-Scott syndrome Heckenlively syndrome Heide syndrome Heliophobia HELLP syndrome ... Houlston-Ironton-Temple syndrome Howard-Young syndrome Howel-Evans syndrome Hoyeraal-Hreidarsson syndrome Hoyeraal syndrome HSV ...
Costello syndrome Encephalocraniocutaneous lipomatosis FG syndrome Hallermann-Streiff syndrome Hydrolethalus syndrome ... Behmel syndrome Sotos syndrome Sturge-Weber syndrome Weaver syndrome Wiedemann-Rautenstrauch syndrome 3C syndrome Glutaric ... Joubert syndrome Keipert syndrome Legius syndrome LEOPARD syndrome Lethal congenital contracture syndrome MASA syndrome ... syndrome; neurocardiofacial-cutaneous syndromes such as Noonan syndrome, Costello syndrome, Gorlin syndrome, (also known as ...
Carter, A. J.; Goldizen, A. W.; Tromp, S. A. (8 April 2010). "Agamas exhibit behavioral syndromes: bolder males bask and feed ... S2CID 242658268.{{cite journal}}: CS1 maint: multiple names: authors list (link) Hallermann, Jacob; Uetz, Peter. "Agama ...
Hallermann's syndrome MeSH C05.116.099.370.231.480 - hypertelorism MeSH C05.116.099.370.231.576 - mandibulofacial dysostosis ... Klippel-Feil syndrome MeSH C05.116.099.370.652 - orofaciodigital syndromes MeSH C05.116.099.370.797 - Rubinstein-Taybi syndrome ... Hallermann's syndrome MeSH C05.660.207.231.480 - hypertelorism MeSH C05.660.207.231.576 - mandibulofacial dysostosis MeSH ... Hajdu-Cheney syndrome MeSH C05.116.099.105 - basal-cell nevus syndrome MeSH C05.116.099.343 - dwarfism MeSH C05.116.099.343.110 ...
Hallermann's syndrome MeSH C16.131.621.207.231.480 - hypertelorism MeSH C16.131.621.207.231.576 - mandibulofacial dysostosis ... MeSH C16.131.077.065 - Alagille syndrome MeSH C16.131.077.095 - Angelman syndrome MeSH C16.131.077.112 - Bardet-Biedl syndrome ... branchio-oto-renal syndrome MeSH C16.131.260.190 - cri du chat syndrome MeSH C16.131.260.210 - De Lange syndrome MeSH C16.131. ... branchio-oto-renal syndrome MeSH C16.320.180.190 - cri du chat syndrome MeSH C16.320.180.210 - De Lange syndrome MeSH C16.320. ...
... syndrome Frontonasal dysplasia with alopecia and genital anomaly Gomez-Lopez-Hernandez syndrome Hallermann-Streiff syndrome ... syndrome Weill-Marchesani syndrome Apert syndrome Carpenter syndrome Microcephaly Pfeiffer syndrome Saethre-Chotzen syndrome ... abnormalities syndrome KBG syndrome Kleefstra syndrome Kohlschutter-Tonz syndrome-like Larsen-like syndrome, B3GAT3 type Lethal ... anomalies-porokeratosis syndrome Crouzon syndrome Crouzon syndrome-acanthosis nigricans syndrome DeSanto-Shinawi syndrome due ...
ATP2C1 Haim-Munk syndrome; 245010; CTSC Hallermann-Streiff syndrome; 234100; GJA1 Hand-foot-uterus Syndrome; 140000; HOXA13 ... AKAP9 Long QT syndrome-3; 603830; SCN5A Long QT syndrome-4; 600919; ANK2 Long QT syndrome-7; 170390; KCNJ2 Long QT syndrome-9; ... TGFBR2 Long QT syndrome 12; 612955; SNT1 Long QT syndrome 13; 613485; KCNJ5 Long QT syndrome-1; 192500; KCNQ1 Long QT syndrome- ... KRAS Noonan syndrome 4; 610733; SOS1 Noonan syndrome 5; 611553; RAF1 Noonan syndrome 6; 613224; NRAS Noonan-like syndrome with ...
Favre-Racouchot syndrome occurs in sun-damaged skin and includes open and closed comedones. Nevus comedonicus or comedo nevus ... Hallermann, C; Bertsch, HP (Jul-Aug 2004). "Two sisters with familial dyskeratotic comedones". European Journal of Dermatology ... Acne is also found premenstrually and in women with polycystic ovarian syndrome. Smoking may worsen acne. Oxidation rather than ...
"Temple-Baraitser Syndrome and Zimmermann-Laband Syndrome: One clinical entity?". BMC Medical Genetics. 17 (1): 42. doi:10.1186/ ... "A homozygous GJA1 gene mutation causes a Hallermann-Streiff/ODDD spectrum phenotype". Human Mutation. 23 (3): 286. doi:10.1002/ ... Common features of Temple-Baraitser syndrome include absent or hypoplastic of finger and toe nails and phalanges and joint ... Mutations in CaV1.2, a voltage gated Ca2+ channel, lead to Timothy syndrome, which causes severe cardiac arrhythmia (long-QT) ...