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Brachymetapody-anodontia-hypotrichosis albinoidism syndrome (anodontia-hypotrichosis syndrome)                                                                                                                                                  169

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Brachymetapody-Anodontia-Hypotrichosis Albinoidism Syndrome (Anodontia-Hypotrichosis
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General: Autosomal recessive.

Ocular: Strabismus; nystagmus; distichiasis; cataracts; high myopia.

Clinical: Congenital anodontia; small maxilla; short stature; shortening of metacarpals and metatarsals; little hair growth; albinoidism.

McKusick VA. Mendelian Inheritance in Man; A Catalog of Human Genes and Genetic Disorders, 12th ed. Baltimore: The Johns Hopkins University Press, 1998.

Online Mendelian Inheritance in Man, OMIM. McKusick-Nathans Institute for Genetic Medicine, Johns Hopkins University and National Center for Biotechnology Information, National Library of Medicine, February 12, 2007. World Wide Web URL: https://www.ncbi.nlm.nih.gov/omim/.

Taumaala P, Haapanen E. Three siblings with similar anomalies in the eyes, bones, and skin. Acta Ophthalmol 1968; 46:365-371.




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