Sweat testing to identify female carriers of X linked hypohidrotic ectodermal dysplasia.
case_report · Level V
Where this comes from
- Record sourced from PubMed, PMID 1865470.
- Also identified by PMC identifier 1016852.
- No licence information is recorded for this record.
- Because redistribution is not established, this page shows the abstract only. Follow the links below for the full text.
Abstract
X linked hypohidrotic ectodermal dysplasia (XHED) affects many epithelial functions, including sweat gland formation. Female carriers who manifest XHED may have defective dentition or a patchy distribution of sweating or both, as determined by starch and iodine sweat testing. Such sweat testing can be useful in assigning carrier status to at risk females in XHED families, and in obtaining an accurate diagnosis for isolated females who present with features of ectodermal dysplasia. The advantages of diagnosing female carriers of XHED include the optimisation of neonatal and paediatric care for affected male infants, who may be at substantial risk of death in infancy.
Medical subject headings
- Ectodermal Dysplasia
- Genetic Carrier Screening
- Iodine
- Starch
- Sweat
- Sweat Glands