Publication: McCune Albright Syndrome: A Case Report
Date
2020
Authors
Article Type
Case Report
Journal Title
Journal ISSN
ISSN 1990-7974 eISSN 1990-7982
Volume Title
Pages
Pages: 134 - 137
Publisher
Nepal Paediatric Society (JNPS)
Abstract
Abstract:
McCune Albright syndrome (MAS) is a very rare genetic disease characterised by any two of the following three findings: café au lait spots, polyosteotic fibrous dysplasia and endocrine disorders. The clinical presentation of MAS may vary depending on which of the various components of the syndrome predominate. Here, we report one case of MAS presenting with precocious puberty.
Description
Subhana Thapa Karki
Department of Paediatrics, Kanti Children’s Hospital, Maharajgunj, Kathmandu, Nepal
Vandana Jain
Department of Paediatrics, All India Institute of Medical Sciences, New Delhi, India
Keywords
Café au lait spots, McCune-Albright syndrome, Polyosteotic fibrous dysplasia, Precocious puberty
Identifier
https://doi.org/10.3126/jnps.v40i2.29099