Diagnosis. Pseudohypoparathyroidism type 1a in a patient with Albright hereditary osteodystrophy, characterized by hypocalcemia, hypothyroidism, growth-hormone deficiency and insulin resistance.

Additionally, research into the NKX2-1 gene has revealed its role in congenital hypothyroidism (CH), a condition that can have severe developmental consequences if not treated early. Genetic ...

The analyses revealed unique genetic variants associated with increased risk of maternal diseases including gestational diabetes, obesity, asthma, psoriasis, endometriosis, and hypothyroidism ...

Because of the unusual association of autoimmune thyroid disease, insulin resistance and obesity rather than insulin deficiency, we searched for possible genetic abnormalities. The HLA haplotypes ...