Temple Syndrome: Clinical Findings, Body Composition and Cognition in 15 Patients

Autor: Alicia F. Juriaans, Gerthe F. Kerkhof, Eva F. Mahabier, Theo C. J. Sas, Nitash Zwaveling-Soonawala, Robbert N. H. Touwslager, Joost Rotteveel, Anita C. S. Hokken-Koelega
Přispěvatelé: Pediatrics, Paediatric Endocrinology, ANS - Cellular & Molecular Mechanisms, ANS - Complex Trait Genetics, AGEM - Amsterdam Gastroenterology Endocrinology Metabolism, Amsterdam Reproduction & Development (AR&D)
Jazyk: angličtina
Rok vydání: 2022
Předmět:
Zdroj: Journal of Clinical Medicine, 11(21):6289. Multidisciplinary Digital Publishing Institute (MDPI)
Journal of clinical medicine, 11(21):6289. Multidisciplinary Digital Publishing Institute (MDPI)
Juriaans, A F, Kerkhof, G F, Mahabier, E F, Sas, T C J, Zwaveling-Soonawala, N, Touwslager, R N H, Rotteveel, J & Hokken-Koelega, A C S 2022, ' Temple Syndrome : Clinical Findings, Body Composition and Cognition in 15 Patients ', Clinical Chemistry, vol. 11, no. 21, 6289 . https://doi.org/10.3390/jcm11216289
Journal of Clinical Medicine; Volume 11; Issue 21; Pages: 6289
Clinical Chemistry, 11(21):6289
ISSN: 2077-0383
0009-9147
Popis: Background: Temple syndrome (TS14) is an imprinting disorder caused by a maternal uniparental disomy of chromosome 14 (UPD(14)mat), paternal deletion of 14q32 or an isolated methylation defect of the MEG3-DMR. Studies on phenotypical characteristics in TS14 are scarce and patients with TS14 often experience delay in diagnosis, which has adverse effects on their health. TS14 is often characterized as either Prader–Willi-like, Silver–Russell-like or as a Silver–Russell spectrum disorder. Methods: This study describes 15 patients with TS14 who visited the Dutch Reference Center for Prader–Willi-like from December 2018 to January 2022. Results: Eight patients had UPD(14)mat and seven a methylation defect. The most common symptoms were intra-uterine growth retardation (IUGR) (100%), hypotonia (100%), precocious puberty (89%), small for gestational age (SGA) birth (67%), tube feeding after birth (53%) and psycho-behavioral problems (53%). Median (interquartile range (IQR)) IQ was 91.5 (84.25; 100.0), whilst many patients were enrolled in special education (54%). The median (IQR) fat mass % (FM%) SDS was 2.53 (2.26; 2.90) and lean body mass (LBM) SDS −2.03 (−3.22; −1.28). There were no significant differences in clinical characteristics between patients with a UPD(14)mat and a methylation defect. Conclusions: Our patients share a distinct phenotype consisting of IUGR, SGA birth, precocious puberty, hypotonia, tube feeding after birth, psycho-behavioral problems and abnormal body composition with a high FM% and low LBM. Whilst similarities with Prader–Willi syndrome (PWS) and Silver–Russell syndrome (SRS) exist, TS14 is a discernible syndrome, deserving a tailored clinical approach. Testing for TS14 should be considered in patients with a PWS or SRS phenotype in infancy if PWS/SRS testing is negative.
Databáze: OpenAIRE
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