Medicine:AREDYLD syndrome

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AREDYLD syndrome
Autosomal recessive - en.svg
AREDYLD syndrome is inherited in an autosomal recessive manner

AREDYLD stands for acral renal ectodermal dysplasia lipoatrophic diabetes. AREDLYD is categorized as a rare disease, meaning it affects fewer than 200,000 people in the United States population at any given time.

It was characterized in 1983.[1] A second case was identified in 1992.[2]

References

  1. "AREDYLD: a syndrome combining an acrorenal field defect, ectodermal dysplasia, lipoatrophic diabetes, and other manifestations.". Am J Med Genet 16 (1): 29–33. 1983. doi:10.1002/ajmg.1320160106. PMID 6638067. 
  2. "Ectodermal dysplasia, lipoatrophy, diabetes mellitus, and amastia: a second case of the AREDYLD syndrome.". Am J Med Genet 44 (3): 374–7. 1992. doi:10.1002/ajmg.1320440321. PMID 1488989. 

External links

Classification
External resources