Search

everythinglearnresearchcommunity

for

Search:↓

A new genetic model may improve treatment and diagnosis for certain inherited skin diseases.

The girl has an inflammatory type of scarring hair loss.

Children with darker skin tones can have specific skin conditions that need tailored treatments.

Melanocytes can regenerate around hair follicles in bullous pemphigoid, especially in patients with darker skin.

Early recognition and treatment of VATS in transplant patients improve outcomes.

Trametinib can cause skin issues, but they can often be managed without stopping the drug.

Connexin 30 is usually absent in normal skin but can appear in certain skin conditions.

Steatocystoma multiplex is a skin condition starting around age 26, linked to hair follicles, and related to eruptive vellus hair cysts.

A 19-year-old man had a rare skin condition on one side of his face that looked like another skin disease.

Punctate follicular porokeratosis is a skin condition with specific features seen in hair follicles.

The report shows that a rare benign tumor was successfully removed from inside the mouth to avoid scarring on the face.

Congenital atrichia is a rare condition where children are born without hair, and treatment is often ineffective.

A 5-year-old boy was diagnosed with congenital triangular alopecia, a type of hair loss without skin changes, usually starting between ages 2-5, with no specific treatment.

Pilomatricomas should be considered to avoid misdiagnosis in children with unusual skin tumors.

Avoiding damage and using specific shampoo and supplements improved the hair condition.

Cantu syndrome, which causes excessive hair growth and skin issues, is due to a mutation in the ABCC9 gene, and understanding this could help develop new treatments for hair diseases.

Molluscum contagiosum can occur in epidermoid cysts, especially with prolonged steroid use.

A 14-year-old girl's black hair showed unique color changes, suggesting early greying.

Facial dark spots can be caused by the sun, genetics, makeup, or medicine, and are diagnosed by patient history and skin tests.

A young boy with a rare skin and nail condition improved significantly with simple topical treatments.

A 4-year-old girl has a rare condition causing hairlessness and skin bumps, but normal teeth and sweating.

Papular acantholytic dyskeratosis of the vulva is a rare, benign skin condition that can be managed conservatively.

An 8-year-old girl has a rare, irreversible hair loss condition caused by a genetic mutation.

A 17-year-old in Saudi Arabia was diagnosed with a rare skin condition causing red-brown facial patches.

Umbilical cord blood transplantation improved the boy's symptoms despite complications.

A 6-year-old girl had both monilethrix and trichorrhexis nodosa, causing brittle hair, with minimal improvement from treatment.

Lipedematous scalp may have a genetic link and could be associated with psychiatric conditions.