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Minoxidil and spironolactone slow hair loss in women.

5α reductase type 2 enzyme mutation and oxidative stress may increase androgenetic alopecia risk in Egyptians.

Two siblings were found to have a genetic condition causing progressive hair loss and woolly hair, which may often be misdiagnosed.

Some human genetic markers work for genetic studies in pig-tailed and stump-tailed macaques, which can help in their conservation.

Mesotherapy is more effective than topical spray for female hair loss treatment.

A Saudi individual initially identified as a girl had a genetic disorder affecting gender development.

Hair growth dysfunction involves various conditions with limited treatment options.

Professor Ma Shuanquan treats hair loss by using Chinese medicine to improve liver, spleen, and kidney health.

PCOS patients, especially obese ones, often lack vitamin D and may need supplements and lifestyle changes.

Dissolvable microneedles with Ginsenoside Rg3 can help treat hair loss by improving drug delivery and stimulating hair growth.

Young women in West Bengal, India, with PCOS often have estrogen resistance, leptin receptor issues, folate deficiency, T2DM, and acanthosis, commonly linked to obesity.

A 27-year-old with APS-1 showed improvement in symptoms after treatment.

Standard treatment for congenital erythropoietic porphyria was ineffective over five years.

Drug repositioning offers hope for new, affordable treatments for a genetic skin disorder called ARCI.

Some skin tumors from hair follicles and glands can be linked to genetic syndromes and may be benign or malignant.

Hashimoto thyroiditis is an autoimmune disease that can lead to an underactive thyroid and is treated with medication and sometimes diet changes or surgery.

PCOS is a common hormonal disorder in women, causing symptoms like acne and irregular periods, and is managed with medication and lifestyle changes.

A new genetic change in the DSC3 gene is linked to a rare condition causing hair loss and skin blisters in a child.

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

A Saudi girl was diagnosed with Loose Anagen Hair Syndrome, a rare condition causing easy hair loss without scarring.

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

Hair restoration can be achieved through non-surgical treatments like minoxidil, antiandrogens, phototherapy, and PRP procedures, or through surgical methods like hair transplantation. Continued treatment is needed to maintain results, and full results are visible after 12-18 months.

Hair loss in young men in Central India is linked to severe heart disease.

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

Vitiligo is often found with other autoimmune diseases, which is important to know to help patients.

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

A 37-year-old male with severe skin and internal issues has a rare inherited skin condition called dystrophic epidermolysis bullosa.

A 56-year-old man was diagnosed with Cronkhite-Canada Syndrome after showing symptoms like diarrhea, weight loss, and skin changes.

A mother and daughter have a rare genetic hair loss disorder with no effective treatment.

Premature greying of hair affects the social lives of medical students but not their self-esteem.