Polydactyly, Postaxial, Type A7; Papa7
Table of contents:
Description
PAPA7 is characterized by postaxial polydactyly restricted to the feet, with well-developed nails present on the extra digits and attachment of both the fifth and sixth toes to a broad 2-headed fifth metatarsal (Umair et al., 2017).For a discussion of genetic heterogeneity of postaxial polydactyly, see {174200}.
Clinical Features
Phenotypes and symptoms related to Polydactyly, Postaxial, Type A7; Papa7
- Syndactyly
- Polydactyly
- Postaxial polydactyly
- Cutaneous syndactyly
- Cubitus varus
Incidence and onset information
— Currently we don't have prevalence information about this disease (Not enough data available about incidence and published cases.)— No data available about the known clinical features onset.
Researches and researchers
Currently, we don't have any information about doctors, researches or researchers related to this disease. Please contact us if you would like to appear here.Polydactyly, Postaxial, Type A7; Papa7 Recommended genes panels
| Panel Name, Specifity and genes Tested/covered |
|---|
 Autism, IQCE related.
By Centogene AG - the Rare Disease Company (Germany).
IQCE
Specificity
100 %
Genes
100 % |
You can get up to -7 more panels with our dedicated tool
Learn moreSources and references
You can check the following sources for additional information.
OMIM Genetic Syndrome FinderIf you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like PROGESTERONE RESISTANCE NEPHRONOPHTHISIS 1; NPHP1