Vol. 20 - Num. 80
Clinical Reviews
Júlia Morata Albaa, Laia Morata Albab, Eva Díez Gandíac
aServicio de Pediatría. Hospital Lluís Alcanyís. Játiva. Valencia. España.
bMédico de Familia. CS Enguera. Departamento Xàtiva-Ontinyent. Valencia. España.
cMIR-Pediatría. Hospital Lluís Alcanyís. Játiva. Valencia. España.
Correspondence: J Morata. E-mail: juliamorataalba@gmail.com
Reference of this article: Morata Alba J, Morata Alba L, Díez Gandía E. What can hide a café-au-lait skin pigmentation? Rev Pediatr Aten Primaria. 2018;20:371-4.
Published in Internet: 12-12-2018 - Visits: 45154
Abstract
McCune-Albright syndrome is a rare sporadic disease, described by McCune and Albright in 1937. It is caused by the mutation of the GNAS1 gene, which stimulates the growth and function of the endocrine glands, melanocytes and osteoclasts. Triad characteristic: polyostotic fibrous dysplasia, multiple endocrine alterations and café-au-lait skin pigmentation.
Keywords
● Café-au-lait skin pigmentation ● Fibrous dysplasia ● McCune-Albright syndrome
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