We have identified a novel interstitial duplication at Xq26.1-q27.3 in a previously reported family with X-linked recessive hypopituitarism [1]. Mapping of the duplication was carried out using interphase FISH analysis of over 60 bacterial genomic clones from Xq25-q28. The proximal and distal breakpoints of the duplication are contained within the 432N13 and 91O18 clones, respectively, and are separated by approximately 9 Mb. Comparison with a recently published 13-Mb duplication in another XH family [2] indicated that the duplication break-points in these families were different. Therefore, we conclude that X-linked hypopituitarism is caused by increased dosage of a gene that is critical for pituitary development and that the causative gene is located within the 9-Mb duplicated region that we have defined.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1006/geno.2002.6741 | DOI Listing |
Rev Endocr Metab Disord
December 2024
Institute of Endocrinology, Rabin Medical Center- Beilinson Hospital, 39 Jabotinksi St, Petach Tikva, 4941492, Israel.
Endocr Rev
September 2024
Department of Endocrinology, Centre Hospitalier Universitaire (CHU) de Liège, University of Liège, Domaine Universitaire Sart Tilman, 4000 Liège, Belgium.
J Clin Res Pediatr Endocrinol
November 2023
İstanbul University, İstanbul Faculty of Medicine, Department of Pediatric Endocrinology, İstanbul, Turkey
IGSF1 deficiency is a rare X-linked condition characterized by central hypothyroidism and a wide variety of other clinical features with variable prevalence, including a delayed pubertal testosterone rise and growth spurt in the context of normal or accelerated testicular growth, and adult macroorchidism with relatively low serum testosterone concentrations. Other features include increased waist circumference, attention deficit, prolactin deficiency and transient partial growth hormone (GH) deficiency in childhood, contrasting with an increased GH secretion in adulthood. Patients with this disorder are not detected shortly after birth if neonatal screening programs are based on thyroid-stimulating hormone (TSH) concentrations.
View Article and Find Full Text PDFBMC Med Genomics
February 2022
Department of Pediatrics, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430030, China.
Background: SOX3 is essential for pituitary development normally at the earliest stages of development. In humans, variants of SOX3 can cause X-linked hypopituitarism with various clinical manifestations, with or without mental retardation.
Case Presentation: We present an 8-year-old Chinese patient with congenital hypopituitarism who had a 6.
Front Oncol
November 2021
Department of Immunology, Genetics and Pathology, Uppsala University, Uppsala, Sweden.
Background: Paraganglioma occurs rarely in the sellar/parasellar region. Here, we report a patient with malignant paraganglioma with primary sellar location with unusual genetic and imaging features.
Case Presentation: A 31-year-old male presented with mild hypertension, headache, nausea, and vomiting.
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!