A Novel Maternally Inherited GNAS Variant in a Family With Hyperphagia and Obesity: 3 Cases.
Anand RamakrishnanDillon PopatPreetha PurushothamanLi F ChanEvelien F GeversPublished in: JCEM case reports (2024)
GNAS variants were recently described in 1% of patients not known to have pseudohypoparathyroidism/inactivating PTH/PTHrP signalling disorder 2 in the UK Genetics of Obesity Study. We describe a new missense GNAS variant, c.791A > C, p.(Asp264Thr), in a family with obesity, hyperphagia and mild PTH resistance. A 6-year-old female (body mass index +4.3 SD score [SDS], height +1.9 SDS) presented with hyperphagia and obesity from age 3 years. She had subtle brachydactyly, macrocephaly, and mildly delayed development. The 12-year-old brother (height +2.1 SDS, body mass index +2.9 SDS) had hyperphagia, obesity, mildly delayed development, and autism. He had subtle brachydactyly, as did the affected mother. We assessed the functional effect of the mutant, measuring cAMP production in cells transfected with wild type and mutant GNAS after ligand stimulation. Cells with the mutant GNAS showed impaired cAMP generation through melanocortin receptor 4, GH releasing hormone receptor, and PTH receptor. These cases demonstrate the clinical heterogeneity of monogenic disease, suggesting a need to test for PHP1A in children with obesity even without classical signs of PHP1A.
Keyphrases
- body mass index
- weight gain
- insulin resistance
- metabolic syndrome
- weight loss
- high fat diet induced
- type diabetes
- wild type
- induced apoptosis
- physical activity
- newly diagnosed
- binding protein
- cell cycle arrest
- end stage renal disease
- autism spectrum disorder
- signaling pathway
- dna methylation
- cross sectional
- copy number
- prognostic factors
- cell proliferation