“…For suspected syndromic HI, based on the clinical assessment or family history, additional tests were performed when applicable, including thyroid hormones (FT4, T3, and TSH), glycemia, serum creatinine level, kidney and thyroid gland ultrasounds, electrocardiography, and/or fundus examination, to refine the diagnosis as described previously in Mali [ 14 ]. For familial or sporadic cases with a putative genetic origin, peripheral blood samples were taken when possible and three-generation pedigrees were drawn using Progeny software (Progeny Genetics LLC, Delray Beach, FL, USA).…”