Open AccessMcCune Albright Syndrome: A Case Report
Author(s) -
Subhana Thapa Karki,
Vandana Jain
Publication year - 2020
Publication title -
journal of nepal paediatric society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.13
H-Index - 8
eISSN - 1990-7982
pISSN - 1990-7974
DOI - 10.3126/jnps.v40i2.29099
Subject(s) - mccune–albright syndrome , medicine , fibrous dysplasia , presentation (obstetrics) , café au lait spot , endocrine system , polyostotic fibrous dysplasia , precocious puberty , pediatrics , pathology , endocrinology , surgery , hormone , neurofibromatosis
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.