Search

everythinglearnresearchcommunity

for

Search:↓

Some children in Malaysia with symptoms have either profound or partial biotinidase deficiency, and early testing and treatment are important.

Trichotillomania is often misdiagnosed as alopecia areata and can be treated effectively with N-acetylcysteine and psychotropic drugs.

A 78-year-old man with Cronkhite-Canada syndrome improved significantly after treatment and remains symptom-free.

Some cases of short anagen hair syndrome are linked to specific genetic variations that are also connected to male pattern baldness.

Steroids, infection management, and nutritional support can significantly improve symptoms of Cronkhite-Canada Syndrome.

Beau's lines on nails may indicate severe COVID-19 or vaccination response.

A man with a weakened immune system was diagnosed with a rare skin condition called trichodysplasia spinulosa using skin examination techniques.

A new syndrome was linked to two new genetic changes in the MBTPS1 gene in a 14-year-old girl.

Eating disorders like anorexia and bulimia cause skin problems, and dermatologists can help detect these disorders early for better treatment outcomes.

The study found that males with KFSD had severe skin and eye symptoms, while female carriers had milder symptoms.

Frontal fibrosing alopecia can mimic traction alopecia but has distinct features like facial papules and eyebrow thinning.

A man's skin condition and poor diet led to a scurvy diagnosis.

The study found two new mutations in a Chinese patient with severe biotinidase deficiency.

Targeted therapies for advanced skin cancer often cause hair and nail problems, which need managing to avoid changing the treatment dose.

Tofacitinib may help treat nail dystrophy, especially when other treatments fail.

Children with partial biotinidase deficiency are healthy at birth but may develop symptoms that improve with biotin therapy.

The document concludes that compulsive hair disorders, like trichotillomania, are complex and require careful diagnosis and treatment from both psychiatric and dermatological perspectives.

Topical vitamin C may help treat skin fragility in the elderly.

Vitamin B12 deficiency can cause skin darkening and white hair, but it's reversible.

A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

A small change in the TRPS1 gene leads to a less severe form of a syndrome affecting hair, nose, and finger development.

Severe nutritional deficiency can cause serious health and development issues, including skin problems and hair loss.

A girl with red hair developed hair-pulling and body image disorders after being bullied for her hair color.

Trichotillomania is a condition where people repeatedly pull out their hair, which can be triggered by stress and has various physical signs.

Most children with pediatric trachyonychia improve over time, regardless of treatment.

Plica neuropathica can be a sign of schizophrenia and improves with antipsychotic treatment.

An 11-year-old girl with a rare skin disorder also had cornea issues and dry eye, needing careful management.

The document concludes that various skin conditions have specific treatments and that adequate calcium intake may prevent osteoporosis.