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Hypotonic male infant and MCT8 deficiency - a diagnosis to think about

Thyroid hormone is crucial in the development of different organs, particularly the brain. MCT8 is a specific transporter of triiodothyronine (T3) hormone and MCT8 gene mutations cause a rare X-linked disorder named MCT8 deficiency, also known as Allan-Herndon-Dudley syndrome, characterized by psychomotor retardation and hypotonia. | Hypotonic male infant and MCT8 deficiency - a diagnosis to think about