An X-linked, recessively inherited syndrome characterized by grave mental deficiency, epilepsy, and endocrine disorder

Acta Med Scand. 1962 Jan;171:13-21. doi: 10.1111/j.0954-6820.1962.tb04162.x.
No abstract available

MeSH terms

  • Endocrinology / genetics*
  • Epilepsy*
  • Face / abnormalities
  • Fingers / abnormalities
  • Growth Disorders*
  • Humans
  • Hypogonadism
  • Intellectual Disability / genetics*
  • Mental Retardation, X-Linked*
  • Obesity
  • Syndrome*

Supplementary concepts

  • Borjeson-Forssman-Lehmann syndrome