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Patients affected by this disorder all share a loss-of-methylation (LOM) at the differentially methylated GNAS exon A\/B, which reduces expression of the stimulatory G protein \u03b1-subunit (Gs\u03b1) from the maternal allele. This leads in the proximal renal tubules, where the paternal GNAS allele does not contribute much to expression of this signaling protein, to little or no Gs\u03b1 expression thereby causing PTH resistance. We now describe a PHP1B patient with a de novo genomic GNAS duplication of approximately 88 kb, which is associated with LOM restricted to exon A\/B alone. Multiplex ligation-dependent probe amplification (MLPA), comparative genomic hybridization (CGH), and whole-genome sequencing (WGS) established that the duplicated DNA fragment extends from GNAS exon AS1 (telomeric breakpoint) to a small region between two imperfect repeats just upstream of LOC105372695 (centromeric breakpoint). Our novel duplication is considerably shorter than previously described duplications\/triplications in that portion of chromosome 20q13 and it does not affect methylation at exons AS and XL. Based on these and previous findings, it appears plausible that the identified genomic abnormality disrupts in cis the actions of a transcript that is required for establishing or maintaining exon A\/B methylation. Our findings extend the molecular causes of PHP1B and provide additional insights into structural GNAS features that are required for maintaining maternal Gs\u03b1 expression and for preventing PTH-resistance. \u00a9 2020 American Society for Bone and Mineral Research (ASBMR).<\/jats:p>","DOI":"10.1002\/jbmr.4209","type":"journal-article","created":{"date-parts":[[2020,11,12]],"date-time":"2020-11-12T17:54:07Z","timestamp":1605203647000},"page":"546-552","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":13,"title":["A Novel GNAS Duplication Associated With Loss-of-Methylation Restricted to Exon A\/B Causes Pseudohypoparathyroidism Type Ib (PHP1B)"],"prefix":"10.1093","volume":"36","author":[{"given":"Monica","family":"Reyes","sequence":"first","affiliation":[{"name":"Endocrine Unit Massachusetts General Hospital and Harvard Medical School Boston MA 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Germany"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Maki","family":"Fukami","sequence":"additional","affiliation":[{"name":"Department of Molecular Endocrinology National Research Institute for Child Health and Development Tokyo Japan"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Harald","family":"J\u00fcppner","sequence":"additional","affiliation":[{"name":"Pediatric Nephrology Unit Massachusetts General Hospital and Harvard Medical School Boston MA USA"},{"name":"Endocrine Unit Massachusetts General Hospital and Harvard Medical School Boston MA USA"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"286","published-online":{"date-parts":[[2020,11,12]]},"reference":[{"issue":"10","key":"2024012713513454800_jbmr4209-bib-0001","doi-asserted-by":"crossref","first-page":"4736","DOI":"10.1210\/jc.2002-020183","article-title":"The gsalpha gene: predominant maternal origin of transcription in human thyroid gland and 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