Congenital hypothyroidism, cerebellar atrophy, and the incomplete phenotypic expression of PHACES syndrome

Endocr J. 2008 Mar;55(1):231; author reply 233. doi: 10.1507/endocrj.k07e-155. Epub 2008 Feb 4.
No abstract available

Publication types

  • Comment
  • Letter

MeSH terms

  • Abnormalities, Multiple / diagnosis*
  • Atrophy
  • Cerebellum / abnormalities
  • Cerebellum / pathology*
  • Female
  • Hemangioma / complications
  • Hemangioma / diagnosis
  • Humans
  • Hyperthyroidism / complications
  • Hyperthyroidism / congenital*
  • Phenotype
  • Skin Diseases / complications
  • Skin Diseases / diagnosis
  • Syndrome