Isolated Congenital Adermatoglyphia
Description
Isolated congenital adermatoglyphia is a rare, genetic developmental defect during embryogenesis disorder characterized by the lack of epidermal ridges on the palms and soles, resulting in the absence of fingerprints, with no other associated manifestations. It is associated with a reduced number of sweat gland openings and reduced transpiration of palms and soles.
Clinical Features
Top most frequent phenotypes and symptoms related to Isolated Congenital Adermatoglyphia
- Flexion contracture
- Clinodactyly
- Hyperhidrosis
- Hyperkeratosis
- Ectodermal dysplasia
- Hypohidrosis
- Pterygium
- Clubbing
- Milia
- Palmar hyperkeratosis
And another 2 symptoms. If you need more information about this disease we can help you.
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.
Alternative names
Isolated Congenital Adermatoglyphia Is also known as congenital absence of fingerprints, immigration delay disease, fingerprints, absence of.
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.Isolated Congenital Adermatoglyphia Recommended genes panels
| Panel Name, Specifity and genes Tested/covered |
|---|
 SMARCAD1.
By Fulgent Genetics Fulgent Genetics (United States).
SMARCAD1
Specificity
100 %
Genes
100 % |
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Learn moreSources and references
You can check the following sources for additional information.
ORPHANET OMIM MESH Genetic Syndrome FinderIf you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 5; HHT5 NEPHROTIC SYNDROME, TYPE 11; NPHS11 D-BIFUNCTIONAL PROTEIN DEFICIENCY