Ectopic Posterior Pituitary, Polydactyly, Midfacial Hypoplasia and Multiple Pituitary Hormone Deficiency due to a Novel Heterozygous IVS11-2A>C(c.1957-2A>C) Mutation in the <italic>GLI2</italic> Gene
A novel heterozygous IVS11-2A>C(c.1957-2A>C) mutation in the GLI2 gene is reported. There was an extremely distinct phenotypical expression in two siblings and their father. The index case was a boy who developed cholestasis and hypoglycaemia in the neonatal period. He had bilateral postaxial...
Main Authors: | Meliha Demiral, Hüseyin Demirbilek, Edip Unal, Ceren Damla Durmaz, Serdar Ceylaner, Mehmet Nuri Özbek |
---|---|
Format: | Article |
Language: | English |
Published: |
Galenos Yayincilik
2020-09-01
|
Series: | JCRPE |
Subjects: | |
Online Access: |
http://www.jcrpe.org/archives/archive-detail/article-preview/ectopic-posterior-pituitary-polydactyly-midfacial-/30877
|
Similar Items
-
Evaluation of the Final Adult Height and Its Determinants in Patients with Growth Hormone Deficiency: A Single-centre Experience from the South-Eastern Region of Turkey
by: Meliha Demiral, et al.
Published: (2020-09-01) -
Identification of a Novel PROP1 Mutation in a Patient with Combined Pituitary Hormone Deficiency and Enlarged Pituitary
by: Laura Penta, et al.
Published: (2019-04-01) -
Distinct pituitary hormone levels of 184 Chinese children and adolescents with multiple pituitary hormone deficiency: a single-centre study
by: Fengxue Wang, et al.
Published: (2019-11-01) -
Combined pituitary hormone deficiency caused by PROP1 mutations: update 20 years post-discovery
by: Fernanda A. Correa, et al.
Published: (2019-05-01) -
Growth without growth hormone in combined pituitary hormone deficiency caused by pituitary stalk interruption syndrome
by: Sang Soo Lee, et al.
Published: (2017-03-01)