2020
DOI: 10.3389/fped.2020.00145
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GNAS, PDE4D, and PRKAR1A Mutations and GNAS Methylation Changes Are Not a Common Cause of Isolated Early-Onset Severe Obesity Among Finnish Children

Abstract: Context: Pseudohypoparathyroidism type Ia (PHP1A) is caused by inactivating mutations involving GNAS exons 1-13, encoding the alpha-subunit of the stimulatory G protein (Gsα). Particularly PHP1A, but also other disorders involving the Gsα-cAMPsignaling pathway, have been associated with early-onset obesity. Thus, patients with mutations in the genes encoding PDE4D and PRKAR1A can also be obese. Furthermore, epigenetic GNAS changes, as in pseudohypoparathyroidism type Ib (PHP1B), can lead to excessive weight. O… Show more

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Cited by 4 publications
(1 citation statement)
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“…There is no single measure of adiposity that can be used across infancy, childhood, and adolescence periods. In the reviewed studies, the definition of overweight or obesity was based: on the weight in infants below 2 years (apart from one study that used weight for adolescents 59 ) and on BMI in children at later ages. A variety of references, including standard references of the International Obesity Task Force (IOTF) or the World Health Organization (WHO), countryspecific growth chart references, or setting-specific reference values were used.…”
Section: Gaps and Constraintsmentioning
confidence: 99%
“…There is no single measure of adiposity that can be used across infancy, childhood, and adolescence periods. In the reviewed studies, the definition of overweight or obesity was based: on the weight in infants below 2 years (apart from one study that used weight for adolescents 59 ) and on BMI in children at later ages. A variety of references, including standard references of the International Obesity Task Force (IOTF) or the World Health Organization (WHO), countryspecific growth chart references, or setting-specific reference values were used.…”
Section: Gaps and Constraintsmentioning
confidence: 99%