Hallermann-Streiff syndrome

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Hallermann-Streiff syndrome
ICD-9 756.0
OMIM 234100
DiseasesDB 32617
MeSH D006210

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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. An organisation supporting people with the Hallermann Streiff Syndrome is the Germany based "Schattenkinder e.V."[1]

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

  1. Germany based Schattenkinder e.V.
  2. 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.
  3. Shiomi T, Guilleminault C, Izumi H, Yamada S, Murata K, Kobayashi T (1999). "Obstructive sleep apnoea in a puerperal patient with Hallermann-Streiff syndrome". Eur. Respir. J. 14 (4): 974–7. PMID 10573253. Unknown parameter |month= ignored (help)
  4. Malde AD, Jagtap SR, Pantvaidya SH (1994). "Hallermann-Streiff syndrome: airway problems during anaesthesia". J Postgrad Med. 40 (4): 216–8. PMID 9136243.
  5. synd/1767 at Who Named It
  6. W. Hallermann. Vogelgesicht und Cataracta congenita. Klinische Monatsblätter für Augenheilkunde, Stuttgart, 1948, 113: 315-318.
  7. E. B. Streiff. Dysmorphie mandibulo-faciale (tête d’oiseau) et alterations oculaires. Ophthalmologica, Basel, 1950, 120: 79-83.

External links

de:Hallermann-Streiff-Syndrom



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