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SHED-CM can reduce hair graying and protect against damage from X-rays.

The document concludes that various hair and scalp disorders in children have specific treatments and proper diagnosis is essential.

Rapp-Hodgkin syndrome, AEC, and EEC are different expressions of the same genetic disorder caused by TP63 gene mutations.

A child with ectodermal dysplasia-syndactyly syndrome has a new mutation in the NECTIN4 gene.

Cronkhite-Canada Syndrome often leads to death within 6-18 months.

The document concludes that over 500 genes are linked to hair disorders and this knowledge is important for creating new treatments.

Monilethrix Syndrome causes fragile, beaded hair that breaks easily and needs early diagnosis for better care.

Hair loss in Clouston's syndrome improved with minoxidil and tretinoin treatment.

Trichoscopy is a useful tool for diagnosing hair disorders without pulling out hair.

Early treatment of children's hair loss, which can be caused by various factors, is important due to its emotional impact.

Taking Propecia might lead to the development of cataracts.

Foxi3 expression in developing teeth and hair is controlled by the ectodysplasin pathway.

Researchers found genetic mutations causing hypohidrotic ectodermal dysplasia in 88% of studied patients and identified new mutations and genetic variations affecting the disease.

A new mutation in the XEDAR gene might cause a rare skin condition called hypohidrotic ectodermal dysplasia.

Strong skin creams work well for long-term scalp inflammation in Rapp-Hodgkin Ectodermal Dysplasia.

Boys with less severe EDA mutations in XLHED have milder symptoms and better sweat and hair production.

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

Giving a special protein to dogs with a certain genetic disease improved their symptoms but didn't help with hair growth.

New gene mutations linked to skin conditions were found, bacteria and chemicals may worsen acne, a dog mutation could exist in humans, virus-like elements might be involved in psoriasis, and a vitamin D3 treatment doesn't prevent chemotherapy-related hair loss.

The gene for Clouston syndrome in a large Indian family is located in the 13q11-q12.1 region.

The review shows that skin symptoms like chronic fungal infections, hair loss, and skin depigmentation are key for early detection and management of APECED.

Lactic acid cream can help improve skin bumps known as eruptive vellus hair cysts.

New biofabrication technologies could lead to treatments for hair loss.

Early diagnosis of Trichorhinophalangeal syndrome type 1 is crucial for treatment and was achieved through clinical examination and family history.

A boy and his father with hereditary hypotrichosis simplex were treated for hair loss, but the treatment result is unknown.

A20 protein is crucial for normal skin and hair development.

Recent progress has been made in understanding inherited hair and nail disorders.

A 2-year-old boy had no hair and unusual organ placement, and it's unclear if it's genetic or coincidental.

An 8-year-old Saudi boy was diagnosed with a rare genetic disorder causing hair loss, skin issues, and light sensitivity.

Hair, teeth, and mammary glands develop similarly at first but use different genes later.