Unknown syndrome in sibs: pili torti, growth delay, developmental delay, and mild neurological abnormalities.
case_report · Level V
Where this comes from
- Record sourced from PubMed, PMID 1379303.
- Also identified by PMC identifier 1016033.
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Abstract
We present male and female sibs of consanguineous parents with features including pili torti with unusual hair shaft electron microscopic (EM) findings, growth delay, developmental delay, and mild to moderate neurological abnormalities. The features of the cases presented here have not been noted in the previously reported clinical syndromes in which pili torti may be found.
Medical subject headings
- Deafness
- Developmental Disabilities
- Growth Disorders
- Hair