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Gene therapy shows promise for treating skin disorders and cancer, but faces technical challenges.

Two sisters have rare hair disorders causing short, fragile, kinky hair.

A woman with CHILD syndrome showed skin abnormalities, and the report suggests CHILD nevus and NEVIL might be the same condition, highlighting the need for diagnosis for genetic advice.

A woman's nail separation was likely caused by poor blood flow, and a treatment for similar conditions might help.

Mimicking growth factors in a topical solution can prolong hair growth phase and reduce hair loss without side effects.

The most common skin problems in Indian children are infections and eczemas.

A gene called Gk5 controls lipid production in the skin and affects hair growth.

Mice are useful for researching human hair loss and testing treatments, despite some differences between species.

The document reports a unique case of woolly hair with a combination of conditions not previously seen together.

Environmental factors can cause mutations in skin proteins, leading to skin disorders.

Steroidogenic isoenzymes may help improve treatments for common hair loss.

The harlequin ichthyosis mouse mutation causes thick skin and early death, resembling a human skin disorder.

Melanoma risk tools need improvement, a gene mutation causes a hair disorder that might be treated by managing cell stress, a potential therapy for a skin-ear disorder involves blocking cell channels, skin wrinkling may indicate lung aging regardless of smoking, and oxidative stress might contribute to common baldness.

New mutations in the SLC39A4 gene found in twins help understand the genetic cause of acrodermatitis enteropathica.

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.

Melanoma risk tools need improvement, certain gene mutations cause skin diseases and could be treated by targeting those mutations, skin wrinkling may relate to lung aging due to genetic factors, and oxidative stress affects hair loss but can be reduced in low oxygen.

Netherton syndrome can cause severe dehydration, infections, and growth issues in infants.

Natural gene therapy shows promise for treating skin disorders like epidermolysis bullosa.

Mutations in three genes cause Uncombable Hair Syndrome, leading to frizzy hair that can't be combed flat.

The absence of functional sebaceous glands causes hair follicle destruction and scarring alopecia.

Men with early hair loss may have a higher risk of enlarged prostate and possibly prostate cancer due to shared hormonal factors.

Mutant mice help researchers understand hair growth and related genetic factors.

Genetic testing confirmed a rare skin disorder in a young girl, which improved with zinc supplementation.

Over half of the children had abnormal hair under a microscope, with many having genetic hair conditions.

Male androgenetic alopecia involves hair follicle miniaturization due to DHT, with potential treatments using inhibitors and blockers.

UVB is good for a skin condition in Asian kids, a lotion works for head lice, a drug helps with a skin blistering disorder, a foam reduces itchiness in skin inflammation, birthmarks can be more widespread, and criteria for a neurocutaneous disorder were agreed upon.

A boy's growth and immune problems were caused by a new mutation in the STAT5B gene.

Injecting triamcinolone into the eyebrow area may help eyelash regrowth in alopecia areata patients.

Transverse sections are better for non-scarring hair loss, vertical sections are better for lichen planopilaris, and either method works for other scarring hair loss types.

A rare ITGB6 gene variant causes intellectual disability, hair loss, and dental issues.