Search

everythinglearnresearchcommunity

for

Search:↓

A 12-year-old girl in Saudi Arabia with Focal dermal hypoplasia showed skin and dental symptoms, highlighting the condition's variability and the need for personalized treatment.

Recognizing congenital triangular alopecia is crucial to avoid unnecessary treatments.

People with Down syndrome are more likely to experience hair loss, and using dermoscopy can help diagnose it.

Temporal triangular alopecia may be linked to sebaceous nevus and shows a new pinkish background feature.

A unique hair tumor with a rippled pattern was identified, showing incomplete differentiation and unusual cell arrangements.

The condition is likely inherited in an autosomal-dominant pattern.

A 39-year-old woman developed uncombable hair syndrome after taking oral contraceptives.

A 5-year-old girl has sparse, dry, and brittle hair but is otherwise healthy.

Cronkhite-Canada syndrome is a rare, non-inherited condition causing various symptoms like polyps, hair loss, and weight loss.

Hair loss in Cronkhite-Canada syndrome may be due to an autoimmune response.

A rare hair follicle disorder can cause itchy, bluish-black bumps on the body.

Proper hair care can prevent and stop hair breakage in people with acquired trichorrhexis nodosa.

A hereditary condition causes hair loss and twisted hair in some family members.

Oral Acitretin effectively resolved symptoms in a child with Netherton syndrome.

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

Cronkhite-Canada syndrome may be more treatable and less severe than previously thought.

Infants with severe KID syndrome may be more prone to serious infections and need close monitoring.

Trichoscopy helps diagnose and monitor the treatment of fungal scalp infections in children.

Keratosis Follicularis Spinulosa Decalvans is a rare genetic disorder causing skin and hair issues, often inherited through the X chromosome.

The document explains how to identify different hair problems using a microscope.

The patient improved significantly after treatment, with only one small scar remaining.

Self-induced hair loss should be considered in patients with androgenetic alopecia.

Hair shaft disorders cause fragile, brittle, and abnormal-looking hair.

A specific gene mutation causes hair loss and potential eye issues, even if vision seems normal.

A 15-year-old girl with hypothyroidism had excess hair and skin issues due to blocked hair follicles.

Sensitive scalp causes discomfort and may relate to hair loss, with treatment focusing on scalp care and medication.

Mutations in the DSG4 gene cause fragile, sparse hair in humans, mice, and rats.

Congenital triangular alopecia can occur outside the typical fronto-temporal region.

Prompt treatment of inflammatory tinea capitis (kerion) is crucial to prevent scarring and hair loss.