Search

everythinglearnresearchcommunity

for

Search:↓

Hair casts on the scalp may be a sign of ongoing pemphigus vulgaris and could suggest a need to adjust treatment.

A PKP1 gene mutation causes skin fragility and hair loss in Chesapeake Bay retriever puppies.

Genetic discoveries are key for understanding, diagnosing, and treating inherited hair and nail disorders.

Nearly half of children with primary immunodeficiency disorders showed skin problems, often as the first sign of their condition.

Changes in keratin affect skin health and can lead to skin disorders like blistering diseases and psoriasis.

The term "Porokeratotic Adnexal Ostial Nevus" is suggested as a more appropriate name.

A child's rare skin disease was triggered by chickenpox.

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

A patient with a PLEC mutation has epidermolysis bullosa, muscular dystrophy, and myasthenia gravis, which improved with steroid treatment.

A 5-year-old girl with a rare genetic disorder, lipoid proteinosis, showed reduced new lesions but persistent scars after avoiding skin trauma.

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

Zinc treatment improved skin and hair issues in a boy with a zinc-related condition.

A boy with monilethrix has brittle hair that breaks easily due to a genetic condition, which might improve by puberty.

A new IL6ST gene variant may cause a unique form of hyper-IgE syndrome with skin abscesses and high IgE levels.

A girl with Turner syndrome had psoriasis, alopecia areata, and trachyonychia.

Congenital atrichia with papular lesions causes permanent hair loss and skin bumps due to a gene mutation.

Early diagnosis and comprehensive management improve life quality for Netherton syndrome patients.

Topical 6% salicylic acid effectively reduced skin plaques in a patient with wooly hair and palmoplantar keratoderma.

Eosinophilic pustular folliculitis should be considered in teens with persistent skin issues for accurate diagnosis and treatment.

Hand-foot-mouth disease may cause nail loss in children.

Monilethrix is a rare hair disorder causing beaded, fragile hair, often improving on its own over time.

Recognizing unusual skin, eye, or hair issues can help diagnose immune system disorders early, especially in children.

Early and accurate diagnosis is crucial for managing rare genetic disorders like this localized variant of junctional epidermolysis bullosa.

Oral etretinate improved hair length and reduced beading in monilethrix.

The child was diagnosed with a skin condition involving inflamed hair follicles.

Patients on long-term hemodialysis often experience severe itching and various skin and nail problems.

Netherton syndrome can cause severe dehydration, infections, and growth issues in infants.

Skin problems are common in thyroid disorders, with dry skin in hypothyroidism and warm, soft skin in hyperthyroidism.

A rare skin condition causing scarring was successfully treated with topical erythromycin and benzoyl peroxide.

The child was diagnosed with cutaneous leishmaniasis.