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MON-265 Congenital Hypothyroidism and Bilateral Ptosis Due to a Novel TSHR Gene Mutation
Author(s) -
Andreea Marinescu,
Francesco De Luca,
Elizabeth A. Suarez
Publication year - 2019
Publication title -
journal of the endocrine society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.046
H-Index - 20
ISSN - 2472-1972
DOI - 10.1210/js.2019-mon-265
Subject(s) - thyroid , dysgenesis , medicine , congenital hypothyroidism , endocrinology , ptosis , family history , levothyroxine , mutation , exon , goiter , gene , biology , genetics , surgery , anatomy

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