Skip navigation

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Results 1 - 10 of 14 for Coarse features
  1. ... of features of the disorder including cognitive impairment, coarse facial features, heart defects, obesity, lung (pulmonary) involvement, short stature, ...
  2. ... characterized by overgrowth of the hands and feet, "coarse" facial features, heart problems, and other abnormalities. Sporadic acromegaly occurs ...
  3. ... fifth (pinky) fingers or toes, and characteristic facial features that are described as coarse. The SMARCB1 gene variants involved in Coffin-Siris ...
  4. ... fifth (pinky) fingers or toes, and characteristic facial features that are described as coarse. The SMARCA4 gene variants involved in Coffin-Siris ...
  5. ... fifth (pinky) fingers or toes, and characteristic facial features that are described as coarse. The ARID1A gene variants involved in Coffin-Siris ...
  6. ... fifth (pinky) fingers or toes, and characteristic facial features that are described as coarse. Most ARID1B gene variants involved in Coffin-Siris ...
  7. ... fifth (pinky) fingers or toes, and characteristic facial features that are described as coarse. Most SMARCE1 gene variants involved in Coffin-Siris ...
  8. ... fifth (pinky) fingers or toes, and characteristic facial features that are described as coarse. Most SOX11 gene variants involved in Coffin-Siris ...
  9. ... hands and soles of the feet (palmoplantar keratoderma); coarse, dry, fine, and tightly curled hair; and a ... have had palmoplantar keratoderma only, without any other features. DSP gene mutations can also cause a potentially ...
  10. ... hands and soles of the feet (palmoplantar keratoderma); coarse, dry, fine, tightly curled, and sometimes sparse hair; ... this gene lead to these different patterns of features.At least one mutation in the JUP gene ...
previous · 1 · 2 · next