ACTA ENDOCRINOLOGICA (BUC)

The International Journal of Romanian Society of Endocrinology / Registered in 1938

in ISI Thomson Master Journal List

July - September 2018, Volume 14, Issue 3
General Endocrinology


Korkmaz HA, Karaarslan U, Eraslan C, Atila D, Hazan F, Barisik V, Ata ES, Etlik O, Yildiz M, Ozkan B

Screening of PROP-1, LHX2 and POU1F1 Mutations in Patients with Ectopic Posterior Pituitary Gland

Acta Endo (Buc) 2018, 14 (3): 300-306
doi: 10.4183/aeb.2018.300

Objective. Ectopic posterior pituitary gland (EPP) is usually characterized by an abnormal pituitary stalk and hypoplasia of the anterior hypophysis. The genetic mechanisms involved in the development of EPP remain uncertain. The aim of this study is to determine whether mutations in the three genes, PROP-1, LHX2, and POU1F1, are associated with the risk for and the characteristics of EPP. Methods. In the Endocrinology Outpatient Clinic of “Dr. Behcet Uz” Children’s Hospital, 27 patients with EPP were submitted to sequencing analyses of the PROP-1, LHX2, and POU1F1 genes. Results. Growth hormone, thyrotropin, corticotropin, gonadotropin, and vasopressin deficiency were observed in 22 (81.5%), 23 (85.2%), 17 (63%), 14 (51.9%), and two (7.4%) patients. Thirteen patients (48.1%) presented with hyperprolactinemia. Fourteen patients (51%) had a history of birth dystocia, and 12 cases (42.1%) had a history of breech presentation. Central nervous system abnormalities included five cases with corpus callosum agenesis, one case with schizencephaly, and one case with Chiari type 1 malformation. We identified a homozygous p.S109* mutation in exon 2 in one male patient with EPP and two different PROP1 gene polymorphisms (A142T or c.109+3 G>A polymorphism) in thirteen patients. Conclusions. Our results suggest that PROP1 gene abnormalities might explain the genetic mechanisms involved in the development of EPP.

Keywords: PROP 1 mutation, ectopic posterior pituitary gland, ectopic neurohypophysis, multiple pituitary hormone deficiency

Correspondence: Huseyin Anil Korkmaz MD, “Dr. Behcet Uz” Children’s Hospital, Division of Pediatric Endocrinology, 1374 St. No.11 Alsancak/Izmir, Izmir, 35210, Turkey, E-mail: hanilkorkmaz@gmail.com