Identification of a novel mutation in TSHR gene in hypothyroid patients in BD

Last updated 10th Dec 2018
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CURATOR

A pinboard by Mst. Noorjahan Begum

PhD student, University of Dhaka & Institute for developing science and health initiatives

PINBOARD SUMMARY

The genetic study will help the patients management by altering treatment strategy

Congenital hypothyroidism (CH) is an endocrine disorder which is characterized by thyroid hormone deficiency at birth. It’s the most common preventable cause of mental retardation resulting from dy...