- Communication
NKX2-5 Variant in Two Siblings with Thyroid Hemiagenesis
- Ewelina Szczepanek-Parulska,
- Bartłomiej Budny,
- Martyna Borowczyk,
- Igor Zhukov,
- Kosma Szutkowski,
- Katarzyna Zawadzka,
- Raiha Tahir,
- Andrzej Minczykowski,
- Marek Niedziela and
- Marek Ruchała
Thyroid hemiagenesis (THA) is an inborn absence of one thyroid lobe of largely unknown etiopathogenesis. The aim of the study was to reveal genetic factors responsible for thyroid maldevelopment in two siblings with THA. None of the family members pr...

