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Monilethrix is a rare, inherited condition causing fragile hair and hair loss, with no cure but some treatments may help.

Steroid treatment improved both gut and nerve symptoms in a man with Cronkhite–Canada syndrome.

Skin cells from people with Epidermolysis Bullosa Simplex have abnormally placed and less active mitochondria.

A novel CLDN1 mutation in a 2-month-old with NISCH showed improvement with symptom management.

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

Stress may cause sudden hair whitening in children.

A girl with Becker naevus syndrome has a genetic variant in the ACTB gene related to her symptoms.

Spiny keratoderma is a rare skin condition with small spines on palms and soles, possibly linked to abnormal hair formation.

A baby's toe was severely damaged by a hair tourniquet, leading to bone and tendon damage, but improved after surgery and treatment.

The woman's skin and hair symptoms were confirmed as frontal fibrosing alopecia, and while facial papules are common in such cases, there's no effective local treatment, but systemic treatments can help.

Uncombable hair syndrome is linked to Zellweger syndrome.

Stress can cause sudden hair whitening in children, but it may reverse on its own.

Nagashima-type palmoplantar keratosis in Asians is caused by a SERPINB7 gene mutation.

Facial trichostasis spinulosa is a chronic condition with significant cosmetic impact, especially in young women.

Stress can cause sudden hair whitening in children, but it may reverse on its own.

Mouse nails are similar to human nails, making them useful for studying nail diseases.

If a child is losing a lot of eyelashes and it keeps happening, doctors should look carefully at their health history because it might be a sign of a different health problem.

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

Low-dose acitretin helps nail psoriasis, stem cells may treat scarring alopecia, Chinese men have lower baldness rates, lateral foldplasty is good for ingrown toenails, hair diameter helps diagnose female baldness, childhood trauma linked to alopecia areata, certain hair-weaving leads to scalp conditions in African American women, and new methods for hair research and understanding hair and sweat gland development were introduced.

Improved oral hygiene and dietary changes can help manage black hairy tongue syndrome.

Enteral supplements can improve symptoms of Cronkhite-Canada syndrome.

The case shows how hard it is to tell apart Multiple Autoimmune Syndrome from other similar autoimmune conditions, but correct diagnosis is key for treatment to work.

Hair loss in Cronkhite-Canada syndrome is reversible by treating the gut issues and doesn't need steroid treatment for the hair itself.

Certain genetic changes in the LSS gene cause a rare skin and hair condition.

The cause of the syndrome with scalp scaling and hair loss is unknown.

Keratosis pilaris is a common skin condition where hair follicles get clogged with keratin, mostly on the arms and thighs.

The family has a unique form of ectodermal dysplasia similar to Clouston syndrome but with different hair and skin symptoms.

Friedreich's ataxia causes thin, weak hair with surface damage and cavities.

New treatments targeting specific genes show promise for treating keratin disorders.