MEHMO, a novel syndrome: assignment of disease locus to Xp21.1-p22.13. Mental retardation, epileptic seizures, hypogonadism and genitalism, microcephaly, obesity

Eur J Hum Genet. 1999 Sep;7(6):621-2. doi: 10.1038/sj.ejhg.5200364.
No abstract available

Publication types

  • Comment
  • Letter

MeSH terms

  • Abnormalities, Multiple*
  • Adolescent
  • Child, Preschool
  • Chromosome Mapping
  • Diagnosis, Differential
  • Electroencephalography
  • Epilepsy / genetics
  • Genetic Linkage
  • Humans
  • Hypogonadism / genetics
  • Infant
  • Intellectual Disability / genetics
  • Male
  • Microcephaly / genetics
  • Obesity / genetics
  • Syndrome
  • X Chromosome*