Article
Homozygous Mutations in Thyroid Peroxidase (TPO) in Hypothyroidism with Intellectual Disability, Developmental Delay, and Hearing and Ocular Anomalies in Two Families: Severe Manifestation of Untreated TPO-deficiency Poses a Diagnostic Dilemma.
The Yale journal of biology and medicine - 1 Sept 2023
Naqvi Syeda Farwa, Yıldız-Bölükbaşı Esra, Afzal Muhammad, Nalbant Gökhan, Mumtaz Sara, Tolun Aslıhan, Malik Sajid
Abstract excerpt
Intellectual disability (ID) involves compromised intellectual, learning and cognitive skills, and behavioral capabilities with reduced psychomotor skills. One of the preventable causes of ID is congenital hypothyroidism (CH), which may be due to biallelic mutations in thyroid peroxidase (TPO). In low- and middle-income countries with no newborn screening programs, CH poses a great risk of ID and long-term...
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