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WNT10A mutations often cause ectodermal dysplasias, with males showing more tooth issues than females.

Hair loss in men is common, treatable, but not curable.

The document concludes that accurate diagnosis of ichthyosis is crucial for treatment and genetic advice, and ongoing research is needed for better therapies.

Inherited ichthyoses cause widespread skin scaling and thickening due to gene mutations.

Androgenetic alopecia involves genetics, hormones, and can be treated with medications or surgery.

Mutations in Gasdermin A3 cause skin inflammation and hair loss by disrupting mitochondria.

Genetic screening is crucial for accurately diagnosing APS-1 due to its varied symptoms.

The document suggests treating individuals with nonclassic congenital adrenal hyperplasia who show symptoms, especially those related to excess male hormones.

Different harmful mutations in the CDH3 gene cause HJMD, but symptoms vary among individuals.

Premature graying of hair may suggest health issues and currently lacks effective treatments.

Non-classic congenital adrenal hyperplasia is a common disorder causing symptoms like acne and infertility, and it's managed based on symptoms, not just test results. Treatment can improve fertility and reduce miscarriage risk.

Mutations in the KRT85 gene cause hair and nail problems.

Low-potency steroids can cause serious side effects in people with skin conditions like Netherton syndrome.

A gene variant in KRT71 causes the curly fur in Selkirk Rex cats.

Kids with early graying hair often have low levels of calcium, ferritin, and vitamin D3.

Woodhouse-Sakati syndrome often causes sexual development issues, hair loss, learning disabilities, deafness, muscle contractions, limb pain, and diabetes.

Finasteride and minoxidil are effective FDA-approved treatments for androgenetic alopecia.

Tigason improved hair growth in a boy with monilethrix without side effects.

Many treatments for hair loss lack proper testing and FDA approval, so their effectiveness is uncertain.

Most treatments for hair loss in 1997 were not effective for most people, and maintaining hair growth was difficult.

Rabbits lacking the Hoxc13 gene show similar hair and skin issues to humans with ECTD-9, making them good for research on this condition.

The document concludes that Rabson-Mendenhall syndrome requires novel treatments for insulin resistance and emphasizes the importance of dental care in affected patients.

Low TRPS1 expression in skin and hair cells is linked to hair problems in Trichorhinophalangeal syndrome.

P-cadherin is important for hair growth and health, and its problems can cause hair and skin disorders.

Haplogroup X found in Altaian population supports Amerindian origin.

Dihydrotestosterone treatment can help penis growth in boys with 5α-reductase deficiency but doesn't fully normalize size after puberty.

A rare benign skin tumor showed unusual features of sebaceous and sweat glands, important for correct diagnosis.

Mutation in hairless gene may increase hair loss risk.

Hair loss is caused by genetics and hormones, diagnosed through examination and biopsy, and treated with medications or surgery.

Loose Anagen Hair Syndrome is found in black-haired Indian children and is often missed, especially in boys.