Watson Syndrome

Watchlist
Retrieved
2021-01-18
Source
Trials
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Genes
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Watson syndrome is an autosomal dominant condition characterized by Lisch nodules of the ocular iris, axillary/inguinal freckling, pulmonary valvular stenosis, relative macrocephaly, short stature, and neurofibromas.Watson syndrome is allelic to NF1, the same gene associated with neurofibromatosis type 1.

See also

  • Westerhof syndrome
  • List of cutaneous conditions