Polydactyly
What's New
Last Posted: Jan 06, 2022
- A genotype and phenotype analysis of SMAD6 mutant patients with radioulnar synostosis.
Shen Fang et al. Molecular genetics & genomic medicine 2021 e1850 - Evaluation of Sporadic and Familial Cases with Craniofrontonasal Syndrome: A Wide Clinical Spectrum and Identification of a Novel EFNB1 Gene Mutation.
Gürsoy Semra et al. Molecular syndromology 2021 12(5) 269-278 - Clinical Genetics of Polydactyly: An Updated Review.
Umair Muhammad et al. Frontiers in genetics 2018 9447 - Absence of tibia with polydactyly
From NCATS Genetic and Rare Diseases Information Center - Brachyphalangy, polydactyly, and tibial aplasia/hypoplasia
From NCATS Genetic and Rare Diseases Information Center - Hypoplasia of the tibia with polydactyly
From NCATS Genetic and Rare Diseases Information Center - Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus syndrome
From NCATS Genetic and Rare Diseases Information Center - Persistence of mullerian derivatives with lymphangiectasia and postaxial polydactyly
From NCATS Genetic and Rare Diseases Information Center - Polydactyly myopia syndrome
From NCATS Genetic and Rare Diseases Information Center - Polydactyly postaxial dental and vertebral
From NCATS Genetic and Rare Diseases Information Center
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
- Page last updated:Apr 18, 2024
- Content source: