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Mandibuloacral dysplasia with type A lipodystrophy

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Description

Mandibuloacral dysplasia with type A lipodystrophy (MADA) is an autosomal recessive disorder characterized by growth retardation, craniofacial anomalies with mandibular hypoplasia, skeletal abnormalities with progressive osteolysis of the distal phalanges and clavicles, and pigmentary skin changes. The lipodystrophy is characterized by a marked acral loss of fatty tissue with normal or increased fatty tissue in the neck and trunk. Some patients may show progeroid features. Metabolic complications can arise due to insulin resistance and diabetes (Young et al., 1971; Simha and Garg, 2002; summary by Garavelli et al., 2009). See also MAD type B (MADB; 608612), which is caused by mutation in the ZMPSTE24 gene (606480).

OMIM

  • Mode of Inheritance

  • Autosomal recessive inheritance

VARIANTS

55

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Genes

External Links

  • OMIM

    248370

  • Orphanet

    90153

  • HPO
  • Medgen

    C5399785

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