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Hallermann–Streiff syndrome Classification and external resources ICD-9 756.0 OMIM 234100 DiseasesDB 32617 MeSH D006210 Hallermann-Streiff syndrome (also known as the François Dyscephalic Syndrome, Hallermann-Streiff-François syndrome, Oculomandibulodyscephaly with hypotrichosis and Oculomandibulofacial syndrome) is a congenital disorder that affects growth, cranial development, hair growth and dental development. There are fewer than 200 people with the syndrome worldwide.[citation needed] An organisation supporting people with the Hallermann Streiff Syndrome is the Germany based "Schattenkinder e.V."[1] Contents 1 Presentation 2 Eponym 3 References 4 External links // Presentation Patients with this syndrome are shorter than the average person and may not develop hair in many places, including in the facial, leg and pubic areas. Patients also have eye problems including clouded or reduced eye size, bilateral cataracts[2] and glaucoma. It can be associated with sleep apnea.[3] It can complicate intubation.[4] Eponym It is named for Wilhelm Hallermann and Enrico Streiff.[5][6][7] References ^ Germany based Schattenkinder e.V. ^ Ertekin V, Selimoğlu MA, Selimoğlu E (2004). "Non-lethal Hallermann-Streiff syndrome with bone fracture: report of a case". Ann. Genet. 47 (4): 387–91. doi:10.1016/j.anngen.2004.03.005. PMID 15581837. http://linkinghub.elsevier.com/retrieve/pii/S000339950400036X.  ^ Shiomi T, Guilleminault C, Izumi H, Yamada S, Murata K, Kobayashi T (October 1999). "Obstructive sleep apnoea in a puerperal patient with Hallermann-Streiff syndrome". Eur. Respir. J. 14 (4): 974–7. doi:10.1034/j.1399-3003.1999.14d42.x. PMID 10573253. http://erj.ersjournals.com/cgi/pmidlookup?view=long&pmid=10573253.  ^ Malde AD, Jagtap SR, Pantvaidya SH (1994). "Hallermann-Streiff syndrome: airway problems during anaesthesia". J Postgrad Med 40 (4): 216–8. PMID 9136243. http://www.jpgmonline.com/article.asp?issn=0022-3859;year=1994;volume=40;issue=4;spage=216;epage=8;aulast=Malde.  ^ synd/1767 at Who Named It? ^ W. Hallermann. Vogelgesicht und Cataracta congenita. Klinische Monatsblätter für Augenheilkunde, Stuttgart, 1948, 113: 315-318. ^ E. B. Streiff. Dysmorphie mandibulo-faciale (tête d’oiseau) et alterations oculaires. Ophthalmologica, Basel, 1950, 120: 79-83. External links Jablonski's Syndrome Database v • d • e Congenital malformations and deformations of face and neck (Q18, 744.4-744.9) Face jaw: Otocephaly mouth: Macrostomia · Microstomia lip: Macrocheilia · Microcheilia chin: Microgenia multiple/other: Hallermann-Streiff syndrome · Branchial cleft cyst Neck Webbed neck M: MOU anat/devp noco/cofa(c)/cogi/tumr, sysi proc (peri), drug (A1) v • d • e Congenital malformations and deformations of musculoskeletal system / musculoskeletal abnormality (Q65–Q76, 754–756.3) Appendicular: Limb/ dysmelia Upper clavicle/shoulder: Cleidocranial dysostosis · Sprengel's deformity · Wallis Zieff Goldblatt syndrome hand deformity: Madelung's deformity · Clinodactyly · Oligodactyly · Polydactyly Lower hip: Dislocation of hip/Hip dysplasia · Upington disease · Coxa valga · Coxa vara knee: Genu valgum · Genu varum · Genu recurvatum foot deformity: varus (Club foot, Pigeon toe) · valgus (Flat feet) · Pes cavus · Rocker bottom foot · Hammer toe Either/both dactyly/digit: Polydactyly/Syndactyly (Webbed toes) · Arachnodactyly · Cenani Lenz syndactylism · Ectrodactyly · Brachydactyly (Clubbed thumb) reduction deficits/limb: Acheiropodia · ectromelia (Phocomelia, Amelia, Hemimelia) multiple joints: Arthrogryposis · Larsen syndrome · Rapadilino syndrome Axial Craniofacial Craniosynostosis: Scaphocephaly · Oxycephaly · Trigonocephaly Craniofacial dysostosis: Crouzon syndrome · Hypertelorism · Hallermann-Streiff syndrome · Treacher-Collins syndrome other: Macrocephaly · Platybasia · Craniodiaphyseal dysplasia · Dolichocephaly · Greig cephalopolysyndactyly syndrome · Plagiocephaly · Saddle nose Vertebral column spinal curvature (Scoliosis) · Klippel-Feil syndrome · Spondylolisthesis · Spina bifida occulta Thoracic skeleton ribs: Cervical rib · Bifid rib sternum: Pectus excavatum · Pectus carinatum M: JNT anat(h/c, u, t, l)/phys noco(arth/defr/back/soft)/cong, sysi/epon, injr proc, drug(M01C, M4) This Genodermatoses article is a stub. You can help Wikipedia by expanding it. v • d • e