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Naxos disease

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Description

In Naxos disease, abnormalities of the skin, hair, and nails are associated with arrhythmogenic right ventricular cardiomyopathy. The ectodermal features are evident from birth or early childhood, whereas the cardiac symptoms develop in young adulthood or later. Clinical variability of ectodermal features has been observed, with hair anomalies ranging from woolly hair to alopecia, and skin abnormalities ranging from mild focal palmoplantar keratoderma to generalized skin fragility or even lethal neonatal epidermolysis bullosa (Protonotarios et al., 1986; Cabral et al., 2010; Pigors et al., 2011; Erken et al., 2011; Sen-Chowdhry and McKenna, 2014). Another syndrome involving cardiomyopathy, woolly hair, and keratoderma (Carvajal syndrome; 605676) is caused by mutation in the desmoplakin gene (DSP; 125647). Also see 610476 for a similar disorder caused by homozygous mutation in the DSC2 gene (125645).

OMIM

  • Mode of Inheritance

  • Autosomal recessive inheritance

VARIANTS

407

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Genes

External Links

  • OMIM

    601214

  • Orphanet

    34217

  • HPO
  • Medgen

    C1832600

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