Ectropion Inferior Cleft Lip And Or Palate
What's New
Last Posted: Mar 09, 2023
- The relation between clinically diagnosed and parent-reported feeding difficulties in children with and without clefts.
Iris A C de Vries et al. European journal of pediatrics 2023 - Brazilian Multiethnic Association Study of Genetic Variant Interactions among FOS, CASP8, MMP2 and CRISPLD2 in the Risk of Nonsyndromic Cleft Lip with or without Cleft Palate.
Machado Renato Assis et al. Dentistry journal 2023 11(1) - Association Between Proton Pump Inhibitor Use During Early Pregnancy and Risk of Congenital Malformations.
Choi Ahhyung et al. JAMA network open 2023 6(1) e2250366 - Genome-wide analysis of copy number variation in humans with cleft lip and/or cleft palate identifies COBLL1, RIC1, and ARHGEF38 as clefting genes.
Lansdon Lisa A et al. American journal of human genetics 2022 - Identification of de novo variants in nonsyndromic cleft lip with/without cleft palate patients with low polygenic risk scores.
Ishorst Nina et al. Molecular genetics & genomic medicine 2022 e2109 - Clinical Applications of Artificial Intelligence and Machine Learning in Children with Cleft Lip and Palate-A Systematic Review.
Huqh Mohamed Zahoor Ul et al. International journal of environmental research and public health 2022 19(17) - The genetic factors contributing to the risk of cleft lip-cleft palate and their clinical utility.
Askarian Saeedeh et al. Oral and maxillofacial surgery 2022 - Craniofacial morphology in Apert syndrome: a systematic review and meta-analysis.
Alam Mohammad Khursheed et al. Scientific reports 2022 12(1) 5708 - 3D Photography to Quantify the Severity of Metopic Craniosynostosis.
Bruce Madeleine K et al. The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association 2022 10556656221087071 - Clinical aspects of 22q11.2 microdeletion syndrome
Szumutku Fanni et al. Orvosi hetilap 2022 163(1) 21-30
More
About Rare Diseases PHGKB
Rare Disease PHGKB is an online, continuously updated, searchable database of published scientific literature, CDC and NIH resources, and other information that address the public health impact and translation of genomic and other precision health discoveries into improved health outcomes related to rare diseases...more
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
- Content source: