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PAON shows skin patterns due to genetic mosaicism.

Laser treatments are the most effective for porokeratotic adnexal ostial nevus.

Acne is a common skin condition linked to diet, hormones, and genetics, and early treatment can prevent scarring.

Early detection of specific skin lesions can help identify Birt-Hogg-Dube syndrome and prevent serious complications.

A 15-year-old with KID syndrome developed a rare skin condition called PEHFN.

Alopecia areata is relatively common in children, has a variable course, and shows different responses to treatment; thyroid testing is recommended for those affected.

The document is a detailed medical reference on skin and genetic disorders.

The document concludes that recognizing and treating cutaneous lupus erythematosus early is crucial for managing the skin and potential systemic symptoms.

Genetics play a role in acne, but how exactly they contribute is not fully understood.

The conclusion is that Pigmented Epithelioid Melanocytoma can start from hair follicle stem cells or from a mole on the skin.

A person was born with both a rare hairless condition and a type of birthmark, which is an uncommon combination.

Moles may stop growing because of cell cooperation, not just because of aging cells.

Moles may stop growing due to cell cooperation, not just because of individual cell aging.

A 12-year-old girl was misdiagnosed with alopecia areata but actually had a nevus sebaceus with a genetic mutation.

Dermoscopy helped correctly diagnose a skin condition that was previously misidentified as a different hair loss disease.

Congenital Triangular Alopecia is a rare, non-scarring hair loss that can be surgically treated in females for cosmetic reasons.

Researchers found a potential new type of skin growth called follicular mucinous nevus.

A man's unusual scalp folds caused by a skin condition were treated with surgery and remained unchanged two years later.

A combined surgical approach by different specialists can effectively treat large birthmarks on the scalp.

The report concludes that atypical Brauer nevus is more common in males, present at birth, and often misdiagnosed due to its unusual scalp locations.

A baby had a unique skin condition with a pale patch and surrounding dark hairs, not linked to other health issues.

A rare skin condition was misdiagnosed as a harmless mole on a woman's eyelid.

A specific mutation known for causing cancer is also found to cause a skin condition in a young girl.

Certain gene variations may increase the risk of alopecia, and platelet-rich plasma treatment can improve hair density in those with hair loss; a rare case of facial Becker's nevus was linked to uneven beard growth.

A man's scalp hair loss was due to a combined melanocytic nevus and alopecia areata, suggesting a possible link between the two conditions.

A woman with CHILD syndrome showed skin abnormalities, and the report suggests CHILD nevus and NEVIL might be the same condition, highlighting the need for diagnosis for genetic advice.

The term "porokeratotic adnexal ostial nevus" is proposed to unify overlapping skin conditions involving eccrine and hair follicles.

A 17-year-old developed woolly hair nevus in adolescence, which is unusual, and over time the hair darkened and straightened slightly, but microscopic changes persisted.

High androgen levels and genetic factors likely cause Becker's nevus and related symptoms.

Spironolactone may help enlarge a small breast linked to Becker's nevus.