Precocious Puberty
What's New
Last Posted: Sep 13, 2024
- The rs6576457 G?>?A variant in the MKRN3 gene promoter significantly increases the risk of central precocious puberty and lung cancer in Hubei Chinese population.
Feng Wu, et al. Human molecular genetics 2024 0 - [Clinical and genetic analysis of three children with Legius syndrome due to variants of SPRED1 gene].
Xi Wang, et al. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2024 0 (8) 941-946 - Understanding the genetic complexity of puberty timing across the allele frequency spectrum.
Katherine A Kentistou, et al. Nature genetics 2024 0 - The Genetic Etiology is a Relevant Cause of Central Precocious Puberty.
Ana Pinheiro Machado Canton, et al. European journal of endocrinology 2024 0 - Association of obesity and menarche SNPs and interaction with environmental factors on precocious puberty.
Peng Xue, et al. Pediatric research 2024 0 - Dual rare genetic diseases in five pediatric patients: insights from next-generation diagnostic methods.
Yupeng Liu, et al. Orphanet journal of rare diseases 2024 0 (1) 159 - MKRN3 circulating levels in girls with central precocious puberty caused by MKRN3 gene mutations.
F Aiello, et al. Journal of endocrinological investigation 2023 0 - The functional study of a novel MKRN3 missense mutation associated with familial central precocious puberty.
Ziwei Chen, et al. American journal of medical genetics. Part A 2023 0 - A comprehensive meta-analysis to identify susceptibility genetic variants for precocious puberty.
Xiuli Gu, et al. Annals of human genetics 2023 0 - Differences in Hyperandrogenism Related to Early Detection of Non-Classical Congenital Adrenal Hyperplasia on Second Newborn Screen.
Bonnie McCann-Crosby, et al. International journal of neonatal screening 2023 0 (3)
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Content Summary
Selected Rare Diseases
- Alpha-1 Antitrypsin Deficiency
- Amyotrophic Lateral Sclerosis
- Brugada Syndrome
- Cerebral Palsy
- Cystic Fibrosis
- Duchenne Muscular Dystrophy
- Eclampsia
- Erythema Multiforme
- Familial Mediterranean Fever
- Fragile X Syndrome
- Gaucher Disease
- Glomerulonephritis
- Graves Disease
- Hemophilia
- Huntington Disease
- Microcephaly
- Myasthenia Gravis
- Phenylketonuria
- Retinitis Pigmentosa
- Severe Combined Immunodeficiency
Disclaimer: Articles listed in the Public Health Knowledge Base are selected by Public Health Genomics Branch to provide current awareness of the literature and news. Inclusion in the update does not necessarily represent the views of the Centers for Disease Control and Prevention nor does it imply endorsement of the article's methods or findings. CDC and DHHS assume no responsibility for the factual accuracy of the items presented. The selection, omission, or content of items does not imply any endorsement or other position taken by CDC or DHHS. Opinion, findings and conclusions expressed by the original authors of items included in the update, or persons quoted therein, are strictly their own and are in no way meant to represent the opinion or views of CDC or DHHS. References to publications, news sources, and non-CDC Websites are provided solely for informational purposes and do not imply endorsement by CDC or DHHS.
- Page last reviewed:Feb 1, 2024
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