Article

Genetic Etiology in Patients Diagnosed With Congenital Hypothroidism With New Generation Sequencing: a Single Center Experience

2022-08-31

Abstract excerpt

<title>Abstract</title> <p><bold>Aim: </bold>Congenital hypothyroidism (CH) is the most common endocrine disorder of the newborn; however, it is seen in every 3000-4000 births (1). The identification of genetic mutations is vital for the continuation of treatment, especially in patients with unidentified dysgenesis and etiology. The present study aims to contribute to the literature sharing the patients of CH wit...

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Literature Corpus work: 663d26cb-2858-593f-9457-a7793fc4e305
DOI: 10.21203/rs.3.rs-1995190/v1

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