[Syndrome of contiguous gene deletions in Xp-21 (deficiency of the glycerol-kinase complex). The association of Duchenne muscular dystrophy, glycerol kinase deficiency and congenital suprarenal hypoplasia]

An Esp Pediatr. 1997 Dec;47(6):639-42.
[Article in Spanish]
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Chromosome Deletion*
  • Chromosomes, Human, Pair 21*
  • Female
  • Gene Deletion*
  • Glycerol Kinase / deficiency*
  • Humans
  • Infant, Newborn
  • Kidney / abnormalities*
  • Male
  • Muscular Dystrophies / complications*
  • Syndrome
  • X Chromosome*

Substances

  • Glycerol Kinase