Английская Википедия:Acro-oto-radial syndrome

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Шаблон:Infobox medical condition

Acro-oto-radial syndrome, also known as Pseudopapilledema blepharophimosis hand anomalies syndrome is a very rare hereditary disorder which is characterized by pseudopapilledema, hearing loss, cranio-facial dysmorphisms and hand/foot anomalies.[1] Unlike other genetic syndromes, people with this syndrome don't exhibit intellectual disabilities. Only 4 cases have been reported in medical literature.[2]

Description

People with this disorder often have the following symptoms:[3]

Cases

The following is the list of all cases of acro-oto-radial syndrome reported in medical literature:

  • 1991: Paes-Alves et al. describes 3 affected members of 2 consanguineous sibships from the same large family in Bahia, Brazil with the symptoms mentioned above. They propose this case to be part of a novel autosomal recessive malformation syndrome.[4]
  • 1997: Bertola et al. describes a 23-year-old patient born to consanguineous parents with the symptoms mentioned above. They conclude that this is also part of the same syndrome reported by Paes-Alves and suggest a name for the syndrome (acro-oto-radial syndrome) [5]

References

Шаблон:Reflist

Шаблон:Genetic-disorder-stub