TLDR A person was born with both a rare hairless condition and a type of birthmark, which is an uncommon combination.
The document reported a rare case of a six-month-old infant with congenital atrichia, characterized by the absence of hair from birth, associated with nevus flammeus, a type of birthmark. The infant, born to consanguineous parents, exhibited complete hair loss on the occipital and temporal regions of the scalp, eyebrows, and eyelashes, with partial hair loss on the parietal and frontal regions. The diagnosis was confirmed through clinical examination and trichoscopy, which showed terminal hair without perifollicular abnormalities. The case was significant as it was the first reported instance of congenital atrichia with nevus flammeus, highlighting the need for further follow-up to monitor potential developments such as papular lesions or neurological issues.
5 citations,
January 2012 in “International journal of trichology” A 2-year-old boy had no hair and unusual organ placement, and it's unclear if it's genetic or coincidental.
8 citations,
January 2011 in “International journal of trichology” Accurate diagnosis of APL is crucial to avoid unnecessary treatments.
32 citations,
January 2005 in “Journal of The American Academy of Dermatology” Some babies are born with alopecia areata, and a treatment with clobetasol propionate can regrow hair in half of the cases.
September 2023 in “International journal of science and healthcare research” Genetic testing is crucial for diagnosing congenital atrichia, a rare condition causing irreversible hair loss.
August 2020 in “Pakistan Journal of Zoology” A new mutation in the Hairless gene causes hair loss in two Pakistani families.
11 citations,
May 2011 in “World Journal of Pediatrics” The document emphasizes the importance of correctly identifying and classifying genetic hair disorders to help diagnose related health conditions.
24 citations,
January 2015 in “Current problems in dermatology” The document concludes that accurate diagnosis of hair loss in children is crucial due to limited treatment options and the condition's psychological impact.
Researchers found a genetic link for hereditary hair loss but need more analysis to identify the exact gene.