LHX4 Gene Alterations: Patient Report and Review of the Literature.

Abstract

LHX4 mutations are rare in combined pituitary hormone deficiency, and even rarer in isolated GHD. We describe a 14 years old boy who was referred for investigation of short stature. Convergent strabismus, nystagmus was present. At the age of 5 years his gait was unstable. A progressive myopathy ensued. Tests of pituitary reserve showed partial IGHD (8.2 ng… (More)

Topics

Cite this paper

@article{Gucev2016LHX4GA, title={LHX4 Gene Alterations: Patient Report and Review of the Literature.}, author={Zoran S. Gucev and Velibor B Tasic and Dijana Plaseska-Karanfilska and Marina Krstevska Konstantinova and Ana Stamatova and Marija Dimishkovska and Nevenka Laban and Momir H. Polenakovic}, journal={Pediatric endocrinology reviews : PER}, year={2016}, volume={13 4}, pages={749-55} }