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An 11-year-old child with total hair loss may have a genetic autoimmune disease, and the outlook for hair regrowth is not good.

Skin lesions in Carney complex are likely caused by a specific group of skin cells that promote pigment production due to a genetic mutation.

The document describes a rare case of IFAP syndrome, a genetic condition with symptoms of hair loss, light sensitivity, and scaly skin.

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

FPHL is a common, age-related, genetic hair loss with unclear causes and limited treatment options.

A new mutation in the STING protein causes a range of symptoms and its severity may be affected by other genetic variations; treatment with a specific inhibitor showed improvement in one patient.

Hair loss in women often doesn't follow a pattern, isn't linked to age, may be genetic, and can be related to thyroid issues or other health factors.

Accurate clinical, histological, and genetic methods are key for understanding and treating hair disorders.

Oral contraceptives lower testosterone levels in women, especially those with certain genetic traits, and may be linked to increased breast cancer risk.

Researchers developed a cost-effective 66 K SNP chip for cashmere goats that is accurate and useful for genetic studies.

Hair microscopy is useful for diagnosing hair disorders, but clear definitions are needed for accurate genetic analysis.

The conference presented findings on how vitamin D levels, genetic factors, and lifestyle choices like smoking and yoga affect various health conditions and diseases.

Diagnosing sex development disorders requires combining medical history, physical exams, imaging, lab tests, and genetic data.

Researchers found new hair and nail genes, how hair reacts to UV, differences in white and pigmented hair growth, nerve changes in alopecia, treatments for baldness and alopecia, a toenail condition linked to a genetic disorder, and that nail fungus is more common in people with psoriasis.

Over 67 genes linked to ichthyosis help improve diagnosis and treatment.

Minoxidil, finasteride, and low-level laser light therapy are effective FDA-approved treatments for hair loss.

The research linked PLCD1 gene variants to the development of trichilemmal cysts.

Researchers found a new gene area linked to male-pattern baldness, which, along with another gene, significantly increases the risk of hair loss in men.

Aromatase gene variation may increase female hair loss risk.

Noggin gene inactivation causes skeletal defects in mice, varying by genetic background.

There's no significant link between the D19S884 marker at the insulin receptor gene and polycystic ovary syndrome.

Hair problems can be caused by genetics or the environment, and treatment should focus on the cause and reducing hair damage.

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

Abnormal scalp whorls can indicate brain development issues but may also be seen in neurologically normal people.

New gene identification techniques have improved the understanding and classification of inherited hair disorders.

A new gene location for Keratosis follicularis squamosa was found on chromosome 7p14.3-7p12.1.

A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

A specific genetic change in the KRT71 gene causes a hair loss condition in Hereford cattle.

A boy's hair that was frizzy and hard to comb returned to normal after 9 months, possibly due to genetic factors.

Acne is a common skin condition linked to diet, hormones, and genetics, and early treatment can prevent scarring.