This corrects the article DOI: 10.1038/nrdp.2017.55.
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http://dx.doi.org/10.1038/nrdp.2017.80 | DOI Listing |
Development
November 2024
MOE Key Laboratory of Model Animal for Disease Study, Model Animal Research Center State Key Laboratory of Pharmaceutical Biotechnology, Nanjing University Medical School, Nanjing 210093, China.
22q11.2 deletion syndrome (22q11.2DS) is the most common chromosomal microdeletion syndrome.
View Article and Find Full Text PDFThe brain-related phenotypes observed in 22q11.2 deletion syndrome (DS) patients are highly variable, and their origin is poorly understood. Changes in brain metabolism might contribute to these phenotypes, as many of the deleted genes are involved in metabolic processes, but this is unknown.
View Article and Find Full Text PDFWorld J Radiol
October 2024
Department of General Medicine, First People's Hospital of Zunyi (Third Affiliated Hospital of Zunyi Medical University), Zunyi 563000, Guizhou Province, China.
Background: Hypoparathyroidism (HP) is a rare endocrine disorder, while situs inversus totalis (SIT) is a rare condition in which the internal organs are positioned in a mirrored pattern compared to their usual positions. This case illustrates some potential shared mechanisms between HP and SIT, highlighting the importance of accurate identification and prompt first emergency, offering insights for future research.
Case Summary: This report discusses a case of a middle-aged patient with adolescent-onset HP with concurrent SIT.
Arch Clin Cases
October 2024
Endocrinology Department, Moineşti Emergency Hospital, 605400 Moineşti, Romania.
Indian J Otolaryngol Head Neck Surg
October 2024
Hearing Disorder Research Center, Loghman Hakim Hospital, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
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