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Related Experiment Videos

[Robinow's syndrome associated with deafness]

A Samoud1, K Menif, M Boulaares

  • 1Service de Pédiatrie, Hôpital La Rabta, Tunis, Tunisie.

Archives Francaises De Pediatrie
|December 1, 1993
PubMed
Summary
This summary is machine-generated.

Robinow mesomelic dysplasia, a rare genetic disorder, can present with hearing loss. This case highlights the association of Robinow mesomelic dysplasia with bilateral sensorineural hearing loss in a child from a consanguineous family.

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Area of Science:

  • Genetics
  • Pediatrics
  • Otolaryngology

Background:

  • Robinow mesomelic dysplasia is a rare genetic disorder.
  • It is characterized by distinctive facial features, limb shortening, and genital hypoplasia.
  • This report details a case with an additional finding of bilateral deafness.