McCune-Albright Syndrome in Infant with Growth Hormone Excess
Background: McCune-Albright is a rare syndrome, caused by mutation of the <i>GNAS1</i> gene, and is characterized by an appearance of multiple endocrinopathies, most commonly premature puberty, polyostotic fibrous dysplasia and skin changes called <i>cafe au lait</i> macules....
Main Authors: | , , , , , |
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Format: | Article |
Language: | English |
Published: |
MDPI AG
2022-07-01
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Series: | Genes |
Subjects: | |
Online Access: | https://www.mdpi.com/2073-4425/13/8/1345 |