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Mutations in the RBPJ gene cause Adams-Oliver Syndrome.

A genetic mutation in the LIPH gene causes hair loss and growth defects.

Epidermolytic ichthyosis can be inherited in a semidominant way with mild symptoms in carriers.

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.

Shorter telomeres in white blood cells may increase the risk of a common type of hair loss.

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

AGA, a common hair loss, is caused by genetics, hormones, age, and environmental factors.

People with PCNT mutations often develop severe insulin resistance and early-onset diabetes during childhood or adolescence.

A Brazilian male with IFAP syndrome has a unique genetic variant causing his condition.

The conclusion is that genetic testing is important for diagnosing and treating various genetic hair disorders.

Gene therapy has potential as a future treatment for Hutchinson-Gilford progeria syndrome.

The document concludes that understanding hair biology is key to treating hair disorders, with gene therapy showing potential as a future treatment.

Mutations in mitochondrial DNA might significantly contribute to the development of Polycystic Ovarian Syndrome.

Prunus mira Koehne is valuable for hair growth and has potential for sustainable use, but needs more research and conservation.

People with Mucopolysaccharidoses often have skin problems like thick skin and extra hair, and recognizing these can help diagnose and treat the condition early.

The cause of alopecia areata is likely a mix of genetics, immune system issues, and environmental factors, with more research needed to understand it fully.

Cats lose fur due to various reasons, including allergies, infections, genetics, hormones, diet, cancer, stress, and some conditions are treatable while others are not.

A new genetic mutation in the TRPV3 gene causes Olmsted-like syndrome in a Mongolian family.

Androgenetic alopecia, or hair loss, is caused by a mix of genetics, hormones, and environment, where testosterone affects hair growth and causes hair to become smaller and grow for a shorter time.

Some congenital hair disorders improve in childhood or with treatments like minoxidil and retinoids, while others like Netherton syndrome and trichothiodystrophy have a poor prognosis.

Early diagnosis and individualized treatment improve outcomes for Congenital Adrenal Hyperplasia.

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

The document concludes that PCOS has a strong genetic component, but more research is needed to fully understand the specific genes involved.

A specific gene variant is linked to a higher risk of hair loss from chemotherapy in breast cancer patients.

Alopecia in patients with epidermolysis bullosa varies in severity and is often caused by skin blistering or trauma.

Understanding skin structure and development helps diagnose and treat skin disorders.

Young HS patients often have other physical and mental health issues, and research on HS covers a wide range of topics including genetics, triggers, treatments, and the need for more data.

Genetic testing can help diagnose skin conditions but needs more research for full effectiveness.

A certain genetic variation in the IL1A gene may lower the risk of a hair loss condition in Chinese people.

Dutasteride injections can help hair growth in androgenic alopecia but need more research for long-term use.