Open AccessA rare case of short stature: Say Meyer syndrome
Author(s) -
TS Karthik,
N. Rajendra Prasad,
Poonam Rani,
Rushikesh Maheshwari,
P Amaresh Reddy,
B. V. S. Chakradhar,
Bindu Me
Publication year - 2013
Publication title -
indian journal of endocrinology and metabolism
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.456
H-Index - 28
eISSN - 2230-9500
pISSN - 2230-8210
DOI - 10.4103/2230-8210.119531
Subject(s) - medicine , short stature , corpus callosum , magnetic resonance imaging , atrophy , synostosis , pediatrics , white matter , surgery , anatomy , radiology , pathology
Say Meyer syndrome is rare X linked condition characterized by developmental delay, short stature and metopic suture synostosis. We are reporting a case of Say Meyer syndrome presented to our hospital for short stature and developmental delay at age 3½ years.