Topical Update
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چکیده
Congenital hypothyroidism is the most common endocrine disease in infants. Through early identification and treatment of affected patients, delays in cognitive and motor development can be effectively prevented. In this topical update, Dr Liz Yuen reviews the aetiology and shares recent advances in understanding the molecular basis of congenital hypothyroidism. Genetic diagnosis and counselling can be provided to affected families regarding prognosis and recurrence risk. We welcome any feedback or suggestions. Please direct them to Dr. Poon Wing Tat (e-mail: [email protected]) of Education Committee, the Hong Kong College of Pathologists. Opinions expressed are those of the authors or named individuals, and are not necessarily those of the Hong Kong College of Pathologists.
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