Phenotypic expansion of POGZ‐related intellectual disability syndrome (White‐Sutton syndrome). Issue 1 (29th November 2019)

• Record Type: Journal Article
• Authors: Assia Batzir, Nurit; Posey, Jennifer E.; Song, Xiaofei; Akdemir, Zeynep Coban; Rosenfeld, Jill A.; Brown, Chester W.; Chen, Emily; Holtrop, Shannon G.; Mizerik, Elizabeth; Nieto Moreno, Margarita; Payne, Katelyn; Raas‐Rothschild, Annick; Scott, Richard; Vernon, Hilary J.; Zadeh, Neda; Lupski, James R.; Sutton, V. Reid
• Is Part Of: American journal of medical genetics. Volume 182:Issue 1(2020)
• Page Start: 38
• Page End: 52
• Publication Date: 2019-11-29
• Subjects: autism -- developmental delay -- intellectual disability -- POGZ -- speech delay; Medical genetics -- Periodicals; 616.14205
• DOI: 10.1002/ajmg.a.61380
• Languages: English
• ISSNs: 1552-4825

Abstract

Abstract: White‐Sutton syndrome (WHSUS) is a recently‐identified genetic disorder resulting from de novo heterozygous pathogenic variants in POGZ . Thus far, over 50 individuals have been reported worldwide, however phenotypic characterization and data regarding the natural history are still incomplete. Here we report the clinical features of 22 individuals with 21 unique loss of function POGZ variants. We observed a broad spectrum of intellectual disability and/or developmental delay with or without autism, and speech delay in all individuals. Other common problems included ocular abnormalities, hearing loss and gait abnormalities. A validated sleep disordered breathing questionnaire identified symptoms of obstructive sleep apnea in 4/12 (33%) individuals. A higher‐than‐expected proportion of cases also had gastrointestinal phenotypes, both functional and anatomical, as well as genitourinary anomalies. In line with previous publications, we observed an increased body mass index (BMI) z‐score compared to the general population (mean 0.59, median 0.9; p 0.0253). Common facial features included microcephaly, broad forehead, midface hypoplasia, triangular mouth, broad nasal root and flat nasal bridge. Analysis of the Baylor Genetics clinical laboratory database revealed that POGZ variants were implicated in approximately 0.14% of cases who underwent clinical exome sequencing for neurological indications with or without involvement of other body systems. This study describes a greater allelic series and expands the phenotypic spectrum of this new syndromic form of intellectual disability and autism.