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Related Experiment Videos

Autosomal dominant ectrodactyly with sensorineural deafness.

P Mishra1, M Muranjan, B A Bharucha

  • 1Department of Pediatrics, K.E.M. Hospital, Parel, Mumbai, India.

Clinical Dysmorphology
|May 29, 2000
PubMed
Summary

This study details a rare family with ectrodactyly (split hand/foot) and severe sensorineural hearing loss (SNHL). The findings suggest a likely autosomal dominant inheritance pattern for this combined condition.

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Area of Science:

  • Medical Genetics
  • Developmental Biology
  • Otolaryngology

Background:

  • Ectrodactyly, or split hand/split foot malformation, is a rare developmental disorder.
  • Congenital hearing loss co-occurring with ectrodactyly is exceptionally rare, with few reported cases globally.
  • This study focuses on a unique family exhibiting both conditions.