Английская Википедия:Infantile systemic hyalinosis

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Шаблон:Infobox medical condition (new) Infantile systemic hyalinosis is an allelic autosomal-recessive condition characterized by multiple skin nodules, hyaline deposition, gingival hypertrophy, osteolytic bone lesions and joint contractures.[1]Шаблон:Rp

Genetics

This disease is caused by mutations in the CMG2 gene (ANTXR2).[2]

Diagnosis

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Management

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See also

References

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External links

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  1. James, William; Berger, Timothy; Elston, Dirk (2005). Andrews' Diseases of the Skin: Clinical Dermatology. (10th ed.). Saunders. Шаблон:ISBN.
  2. Шаблон:Cite journal