Conditions / Endocrine

congenital nongoitrous hypothyroidism 6

info · Endocrine · ICD-10: E03.1

A congenital hypothyroidism that has_material_basis_in heterozygous mutation in the THRA gene on chromosome 17q21.1.

Signs and symptoms

  • Congenital hip dislocation
  • Increased body weight
  • Broad-based gait
  • Delayed eruption of teeth
  • Increased body mass index
  • Delayed skeletal maturation
  • Relative macrocephaly
  • Increased T3/T4 ratio
  • Dry skin
  • Anemia

Also known as: CHNG6