myICD10.com Logo
rothmund-thomson syndrome

Medical Definition

An autosomal recessive syndrome occurring principally in females, characterized by the presence of reticulated, atrophic, hyperpigmented, telangiectatic cutaneous plaques, often accompanied by juvenile cataracts, saddle nose, congenital bone defects, disturbances in the growth of hair; nails; and teeth; and hypogonadism.
Related Codes (1)
Code
Description
Billable
Details
Q82.8Other specified congenital malformations of skin
Type 1 Excludes (1)

Rows per page

Page 1 of 1