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Gastric bypass surgery improved a woman's hormonal disorder without the need for medication.

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

Certain genes and X chromosome patterns may significantly contribute to the development of hair loss.

A boy with chromosome 13q deletion syndrome developed eye cancer, a woman with breast cancer lost vision due to a rare side-effect of her treatment, a man's vision worsened after using a hair loss drug, and two rare disorders were discussed. Optical Coherence Tomography is useful for diagnosing and monitoring these conditions.

Chromosomal differences affect how muscle cells respond to testosterone.

Certain gene variations and irregular X chromosome activity may contribute to hair loss in women who can have children.

Certain changes in the VEGF gene can increase or decrease the risk of polycystic ovary syndrome.

Genetic testing confirmed a young girl has Atrichia with Papular Lesions due to mutations in the hairless gene.

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.

A defective gene causes hair loss and taste insensitivity in BTBR mice.

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

Researchers found a genetic region that influences the number of coat layers in dogs.

Using a combination of specific cell cycle regulators is better for safely keeping hair root cells alive indefinitely compared to cancer-related methods.

Environmental factors like smoking, UV exposure, and poor diet contribute to hair loss and graying, and lifestyle changes can help manage it.

Certain genes are linked to the risk of developing Alopecia Areata.

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

Reversing female hair loss.

Researchers found a new mutation in the FERMT1 gene in a Spanish family with Kindler syndrome.

A 12-year-old boy with a rare genetic condition has progressive hair loss with no effective treatment.

A 6-year-old girl with Turner syndrome also had psoriasis, alopecia areata, and trachyonychia.

Genetic testing is crucial for diagnosing congenital atrichia, a rare condition causing irreversible hair loss.

The document concludes that current treatments for androgenic alopecia are not fully effective, but new therapies like botulinum toxin and PRP show promise, and future gene therapy could be beneficial.

BAY 43-9006 helps control kidney cancer growth but doesn't significantly increase overall survival.

Certain mutations in the H6PD gene cause Cortisone Reductase Deficiency by affecting hormone production.

Researchers found a new mutation causing total hair loss from birth.

Longer GGN repeats in the androgen receptor gene are linked to polycystic ovary syndrome.

The most different genetic segment between Africans and East Asians is the EDA2R/AR region, with two main types influenced by population changes and natural selection, and linked to baldness.

The hair keratin gene KRT81 is found in both normal and breast cancer cells and helps them invade surrounding tissues.

KLF4 is important for maintaining skin stem cells and helps heal wounds.

The X5 Hairlaser might help treat male hair loss, but more research is needed.