Intrahepatic Cholestasis Of Pregnancy
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Last Posted: Sep 20, 2024
- Genetic issues in ICP.
Julia Zöllner, et al. Obstetric medicine 2024 0 (3) 157-161 - Associations between ALDOB polymorphisms and intrahepatic cholestasis of pregnancy susceptibility in the Chinese Han population.
Xianxian Liu, et al. Ginekologia polska 2023 0 - MDR3 rs2109505 and rs1202283 polymorphisms are associated with susceptibility to intrahepatic cholestasis of pregnancy: A meta-analysis.
Haiyan Zhuo, et al. Advances in clinical and experimental medicine : official organ Wroclaw Medical University 2023 0 - ABCB4 Gene Aberrations in Human Liver Disease: An Evolving Spectrum.
Reichert Matthias Christian, et al. Seminars in liver disease 2018 0 (4) 299-307 - Pruritus in Pregnancy and Its Management.
Bechtel Mark A, et al. Dermatologic clinics 2018 0 (3) 259-265 - Genetic contribution of ABCC2 to Dubin-Johnson syndrome and inherited cholestatic disorders.
Corpechot Christophe, et al. Liver international : official journal of the International Association for the Study of the Liver 2019 0 (1) 163-174 - Contraceptive vaginal ring-induced cholestasis in a patient with a history of intrahepatic cholestasis of pregnancy.
Perrault Florence, et al. Clinics and research in hepatology and gastroenterology 2020 0 (4) 101475 - Common ABCB4 and ABCB11 Genotypes Are Associated with Idiopathic Chronic Cholestasis in Adults.
Jüngst Christoph, et al. Digestive diseases (Basel, Switzerland) 2021 0 (4) 489-496 - Effect of intrahepatic cholestasis of pregnancy on infantile food allergy: A retrospective longitudinal study cohort in Southwest China.
Huang Liqiong, et al. European journal of obstetrics, gynecology, and reproductive biology 2022 0 110-115 - Identification of two novel pathogenic variants of the NR1H4 gene in intrahepatic cholestasis of pregnancy patients.
Lai Hua, et al. BMC medical genomics 2022 0 (1) 90
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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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