Familial GATA6 mutation causing variably expressed diabetes mellitus and cardiac and renal abnormalities. (3rd May 2019)

• Record Type: Journal Article
• Authors: Du, Yang Timothy; Moore, Lynette; Poplawski, Nicola K; De Sousa, Sunita M C
• Is Part Of: Endocrinology, diabetes & metabolism case reports. (2019)
• Publication Date: 2019-05-03
• Subjects: Adult -- Male -- White -- Australia; Heart -- Kidney -- Pancreas -- Pituitary -- Cardiovascular endocrinology -- Developmental endocrinology -- Diabetes -- Genetics and mutation -- Paediatric endocrinology -- GH -- Insulin -- Gonadotropins -- Hypogonadism -- Neonatal diabetes -- Growth hormone deficiency (adult); Proteinuria -- Umbilical hernia -- Cognitive problems -- Facies - abnormal -- Hypogonadism -- Growth hormone deficiency -- Facial plethora -- Renal biopsy -- Histopathology -- Genetic analysis -- DNA sequencing -- Molecular genetic analysis -- Immunostaining -- Haematoxylin and eosin staining; Cardiology -- Genetics -- Paediatrics -- Urology; New disease or syndrome: presentations/diagnosis/management -- May -- 2019; Endocrinology -- Periodicals; Diabetes -- Periodicals; Diabetes Mellitus; Endocrinology; Diabetes; Endocrinology; Case Reports; Periodicals; Periodicals; 616.4
• DOI: 10.1530/EDM-19-0022
• Languages: English
• ISSNs: 2052-0573

Abstract

Summary: A 26-year-old man presented with a combination of permanent neonatal diabetes due to pancreatic aplasia, complex congenital heart disease, central hypogonadism and growth hormone deficiency, structural renal abnormalities with proteinuria, umbilical hernia, neurocognitive impairment and dysmorphic features. His older brother had diabetes mellitus due to pancreatic hypoplasia, complex congenital heart disease, hypospadias and umbilical hernia. Their father had an atrial septal defect, umbilical hernia and diabetes mellitus diagnosed incidentally in adulthood on employment screening. The proband's paternal grandmother had a congenital heart defect. Genetic testing of the proband revealed a novel heterozygous missense variant (Chr18:g.19761441T>C, c.1330T>C, p.Cys444Arg) in exon 4 of GATA6, which is class 5 (pathogenic) using American College of Medical Genetics and Genomics guidelines and is likely to account for his multisystem disorder. The same variant was detected in his brother and father, but not his paternal grandmother. This novel variant of GATA6 likely occurred de novo in the father with autosomal dominant inheritance in the proband and his brother. The case is exceptional as very few families with monogenic diabetes due to GATA6 mutations have been reported to date and we describe a new link between GATA6 and renal pathology. Learning points: Monogenic diabetes should be suspected in patients presenting with syndromic features, multisystem congenital disease, neonatal-onset diabetes and/or a suggestive family history. Recognition and identification of genetic diabetes may improve patient understanding and empowerment and allow for better tailored management. Identification of a genetic disorder may have important implications for family planning.