search

MeSH 搜索器

Donohue Syndrome

Rare autosomal recessive syndrome of extreme insulin resistance due to mutations in the binding domain of INSULIN RECEPTOR. Clinical features include severe intrauterine and postnatal growth restriction, characteristic dysmorphic FACIES; HIRSUTISM; VIRILIZATION; multiple endocrine abnormalities, and early death.
推出的年份: 2010
副标题
树号: C05.660.207.325, C16.131.077.313, C16.320.215, C18.452.394.750.654, C19.246.537
MeSH 单一 ID: D056731
进入的组:
  • Syndrome, Donohue
  • Leprechaunism
  • Leprechaunisms
  • Rabson-Mendenhall Syndrome
  • Rabson Mendenhall Syndrome
  • Syndrome, Rabson-Mendenhall
  • Mendenhall Syndrome
  • Syndrome, Mendenhall
  • Pineal Hyperplasia, Insulin-Resistant Diabetes Mellitus, And Somatic Abnormalities
早前的内容:
  • Abnormalities, Multiple (2002-2009)
  • Acanthosis Nigricans (2002-2009)
  • Diabetes Mellitus (2000-2009)

留言 (0)

沒有登入
gif