Hallermann–Streiff syndrome

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Hallermann–Streiff syndrome
Other namesOculomandibulofacial syndrome, François dyscephalic syndrome, Hallermann–Streiff–François syndrome, Oculomandibulodyscephaly with hypotrichosis, Aubry syndrome, Ullrich-Fremery-Dohna syndrome
SpecialtyMedical genetics Edit this on Wikidata

Hallermann–Streiff 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 organization supporting people with Hallermann–Streiff syndrome is the Germany-based "Schattenkinder e.V."[1]


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 reduced eye size, bilateral cataracts[2] and glaucoma. The syndrome can be associated with sleep apnea.[3] The physical characteristics of the syndrome can result in difficult intubation by medical professionals.[4] Intelligence is usually normal.[5]


The genetic cause of Hallermann–Streiff syndrome has not been conclusively determined. It is most likely due to a de novo mutation,[6] and it may be associated with the GJA1 gene.[7]


Diagnosis is based on the physical characteristics and symptoms.[5] There is no established clinical genetic testing for Hallermann–Streiff syndrome, however some laboratories offer research genetic testing for the condition.[6]


There is no cure for Hallermann–Streiff syndrome. Treatments centre around the particular symptoms in each individual. Early measures are based around ensuring proper breathing and intake of nutrients and may include a tracheostomy. Early surgery for cataracts may be recommended, however some studies have suggested that spontaneous resolution of cataracts occurs in up to 50% of untreated patients. Regular visits to an ophthalmologist to monitor and deal with other eye problems, some of which may require surgery, are strongly recommended.[6]

Management of the condition may also include surgical reconstruction of certain craniofacial malformations (particularly in the mandibular and nasal region) at an appropriate age. Additionally, management for certain heart defects, such as medication or surgery, may be needed.[6]


It is named after German ophthalmologist Wilhelm Hallermann (1909–2005) and Italian-Swiss ophthalmologist Enrico Bernardo Streiff (1908–1988),[8][9][10] who first described the syndrome in 1948 and 1950 respectively.[11]


  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 (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.
  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. ^ a b "Hallermann-Streiff syndrome - Natural Living Center". www.naturallivingcenter.net. Retrieved 2018-03-05.
  6. ^ a b c d "Hallermann-Streiff syndrome | Genetic and Rare Diseases Information Center (GARD) – an NCATS Program". rarediseases.info.nih.gov. Retrieved 2018-03-05.
  7. ^ Pizzuti A, Flex E, Mingarelli R, Salpietro C, Zelante L, Dallapiccola B (March 2004). "A homozygous GJA1 gene mutation causes a Hallermann-Streiff/ODDD spectrum phenotype". Hum. Mutat. 23 (3): 286. doi:10.1002/humu.9220. PMID 14974090.
  8. ^ synd/1767 at Who Named It?
  9. ^ W. Hallermann. Vogelgesicht und Cataracta congenita. Klinische Monatsblätter für Augenheilkunde, Stuttgart, 1948, 113: 315–318.
  10. ^ E. B. Streiff. Dysmorphie mandibulo-faciale (tête d’oiseau) et alterations oculaires. Ophthalmologica, Basel, 1950, 120: 79–83.
  11. ^ Wynbrandt, James; Ludman, Mark D. (2010-05-12). The Encyclopedia of Genetic Disorders and Birth Defects. Infobase Publishing. p. 185. ISBN 9781438120959.

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