- Cockayne syndrome: a case with hyperinsulinemia and growth hormone deficiency
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Park SK, Chang SH, Cho SB, Baek HS, Lee DY
- KMID: 1422190
- J Korean Med Sci.
- 1994 Feb;9(1):74-77.
- doi: 10.3346/jkms.1994.9.1.74
Cockayne syndrome is a rare autosomal recessive disorder of childhood characterized by cachectic dwarfism with senile-like appearance, mental retardation, photosensitive dermatitis, loss of adipose tissue, pigmentary degeneration of retina, microcephaly,... -
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