A Case of Short Stature and Severe Osteoporosis in a Young Man with Oculocutaneous Albinism: Syndrome or Coincidence?

Oculocutaneous albinism (OCA) is a rare autosomal recessive congenital condition characterized by reduced or absent production of the pigment melanin by melanocytes. The affected individuals have increased susceptibility to sunburn and skin cancers. Osteoporosis is a disease entity characterized by...

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Detalles Bibliográficos
Autor principal: Oyibo, Samson O
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2020
Materias:
Dermatology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7186092/
https://www.ncbi.nlm.nih.gov/pubmed/32351865
http://dx.doi.org/10.7759/cureus.7817

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7186092/
https://www.ncbi.nlm.nih.gov/pubmed/32351865
http://dx.doi.org/10.7759/cureus.7817

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