McCune-Albright syndrome without endocrine dysfunction: Case report in a young boy

Authors

  • Elkashif Sami
  • Agrawal Pankaj

DOI:

https://doi.org/10.32677/IJCH.2017.v04.i04.047

Keywords:

Fibrous dysplasia, McCune-Albright syndrome, Polyostotic

Abstract

The McCune-Albright syndrome (MAS) is a sporadic rare disease characterized by a triad of physical signs: Café-au lait spots, polyostotic fibrous dysplasia, and autonomous endocrine hyperfunction. Based on the studies, it can be concluded that this syndrome is caused by mutations that happen in the gene: GNAS1. A small number, but not all, of the patient’s cells contain this faulty gene (mosaicism). MAS is predominantly observed in girls and is rarely reported in males. We report a 5-year-old boy with café-au-lait spots, polyostotic fibrous dysplasia, and without any endocrine dysfunction.

Downloads

Download data is not yet available.

Downloads

Published

2017-12-25

How to Cite

McCune-Albright syndrome without endocrine dysfunction: Case report in a young boy. (2017). Indian Journal of Child Health, 4(4), 649-651. https://doi.org/10.32677/IJCH.2017.v04.i04.047

Most read articles by the same author(s)

<< < 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 > >>