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A specific mutation in the K25 gene causes a rare genetic disorder with curly hair at birth and later hair loss, along with dental issues.

A TP63 gene mutation causes significant hair loss and mild skin, nail, and tooth abnormalities.

A specific gene variant is linked to heart disease, increased heart muscle, curly hair, and thick skin on palms and soles.

Studying rare genetic disorders can help us understand and treat common diseases better.

A specific gene mutation causes Olmsted syndrome.

Early diagnosis of Trichorhinophalangeal syndrome type 1 is crucial for treatment and was achieved through clinical examination and family history.

The new rodent model successfully mimics non-lean human PCOS symptoms.

A condition with certain scalp changes may come before acne keloidalis nuchae and other similar hair loss disorders.

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

A new tool can analyze hair to detect changes due to hormones, genetics, and aging.

Genetic analysis of rabbits identified key genes for traits like coat color, body size, and fertility.

Different types of PCOS need specific diagnosis methods and treatments.

Early genetic testing and JAK inhibitors can help treat systemic inflammation in SAVI patients.

Melanoma characteristics vary by age, which could help doctors with diagnosis and prevention.

Get3d protein helps maintain photosynthesis in plants and photosynthetic bacteria.

A new genetic change in the keratin 10 gene caused a skin condition called ichthyosis hystrix in a father and his daughter.

The Wnt signaling pathway is not a major factor in the development of keratoacanthoma, a type of skin tumor.

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.

5α-Reductase inhibitors can help treat hair loss, acne, and prostate issues by reducing DHT levels.

The document concludes that managing PCOS requires a comprehensive approach, including lifestyle changes and medication, to improve symptoms and reduce health risks.

Brazilian women with PCOS and both menstrual irregularity and high male hormone levels have a higher chance of having metabolic syndrome.

A gene deletion causes the "hairless" trait in Iffa Credo rats.

Hormones and genetics play key roles in male and female baldness, which can affect mental health and may be linked to other health issues.

The document explains the difficulty in diagnosing and treating brain diseases caused by the immune system and stresses the need for quick and accurate tests.

The p.P25L mutation in the KRT5 gene causes a rare skin condition that worsens over time and may lead to hair loss starting in young adulthood.

Terbinafine can cause hair loss.

A new one-step test can quickly identify skin cancer during surgery.

Topical glucocorticoids thin the skin and change collagen structure.

HPH-15, a new compound, effectively reduces skin fibrosis in experiments without causing harm.