Novel Splicing Mutation in B3GAT3 Associated with Short Stature, GH Deficiency, Hypoglycaemia, Developmental Delay, and Multiple Congenital Anomalies. (28th November 2017)
- Record Type:
- Journal Article
- Title:
- Novel Splicing Mutation in B3GAT3 Associated with Short Stature, GH Deficiency, Hypoglycaemia, Developmental Delay, and Multiple Congenital Anomalies. (28th November 2017)
- Main Title:
- Novel Splicing Mutation in B3GAT3 Associated with Short Stature, GH Deficiency, Hypoglycaemia, Developmental Delay, and Multiple Congenital Anomalies
- Authors:
- Bloor, Samuel
Giri, Dinesh
Didi, Mohammed
Senniappan, Senthil - Other Names:
- Ban Yoshiyuki Academic Editor.
- Abstract:
- Abstract : B3GAT3, encoding β -1, 3-glucuronyltransferase 3, has an important role in proteoglycan biosynthesis. Homozygous B3GAT3 mutations have been associated with short stature, skeletal deformities, and congenital heart defects. We describe for the first time a novel heterozygous splice site mutation in B3GAT3 contributing to severe short stature, growth hormone (GH) deficiency, recurrent ketotic hypoglycaemia, facial dysmorphism, and congenital heart defects. A female infant, born at 34 weeks' gestation to nonconsanguineous Caucasian parents with a birth weight of 1.9 kg, was noted to have cloacal abnormality, ventricular septal defect, pulmonary stenosis, and congenital sensorineural deafness. At 4 years of age, she was diagnosed with GH deficiency due to her short stature (height < 2.5 SD). MRI of the pituitary gland revealed a small anterior pituitary. She has multiple dysmorphic features: anteverted nares, small upturned nose, hypertelorism, slight frontal bossing, short proximal bones, hypermobile joints, and downslanting palpebral fissures. Whole exome sequencing (WES) was performed on the genomic DNA from the patient and biological mother. A heterozygous mutation in B3GAT3 (c.888+262T>G) in the invariant "GT" splice donor site was identified. This variant is considered to be pathogenic as it decreases the splicing efficiency in the mRNA.
- Is Part Of:
- Case reports in genetics. Volume 2017(2017)
- Journal:
- Case reports in genetics
- Issue:
- Volume 2017(2017)
- Issue Display:
- Volume 2017, Issue 2017 (2017)
- Year:
- 2017
- Volume:
- 2017
- Issue:
- 2017
- Issue Sort Value:
- 2017-2017-2017-0000
- Page Start:
- Page End:
- Publication Date:
- 2017-11-28
- Subjects:
- Genetics -- Periodicals
Genetics -- Case studies -- Periodicals
Genetics
Genetic Phenomena
Genetics
Periodicals
Case studies
Periodicals
Case Reports
Fulltext
Internet Resources
Periodicals
576.5 - Journal URLs:
- https://www.hindawi.com/journals/crig/ ↗
http://bibpurl.oclc.org/web/48973 ↗
http://www.ncbi.nlm.nih.gov/pmc/journals/1908/ ↗
http://search.ebscohost.com/direct.asp?db=a9h&jid=%22EGT6%22&scope=site ↗ - DOI:
- 10.1155/2017/3941483 ↗
- Languages:
- English
- ISSNs:
- 2090-6544
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library HMNTS - ELD Digital store
- Ingest File:
- 22490.xml