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Patients often experience long-lasting changes to their hair after stem cell transplants.

Hormones, especially testosterone and DHT, are key for penis development and function, and testosterone therapy may help with erectile dysfunction in those with low levels.

Blond hair in Solomon Islanders is due to a unique genetic variant, not European ancestry.

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

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

Surgery on a baby with a skin disorder improved eyelid position and eye health.

The document concludes that Borrelia afzelii causes a skin condition in France, a gene is linked to hair loss in Caucasian women, and various genetic mutations affect skin diseases.

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.

Changing the environment around stem cells could help tissue repair, but it's hard to be precise and avoid side effects.

The definition of Polycystic Ovary Syndrome may change with new research, and careful screening is key for managing the condition.

TNF family proteins are crucial for the development of skin features like hair, teeth, and mammary glands.

Coats' Plus is a genetic disorder with eye abnormalities, brain calcification, poor growth, bone and skin issues, and movement disorders.

Researchers created a new mouse model for studying Citrullinemia Type I and similar conditions, showing symptoms and treatment responses like those in humans.

People who carry the 21-Hydroxylase Deficiency gene are not more likely to have excessive male hormone levels.

Finasteride irreversibly affects human steroid 5α-reductase 2, providing insight into its catalytic mechanism and disease-related mutations.

Women with excessive male-pattern hair growth should get a full hormone check-up to find and treat any underlying issues, considering both medical and emotional aspects.

Proper control of β-catenin activity is crucial for development and preventing diseases like cancer.

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

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

The monkey's hair loss was due to an autoimmune disease, not genetics.

Hair loss in certain young mice is linked to a specific gene and can be caused by lack of iron.

Vitamin D receptor can control the hairless gene linked to hair loss even without vitamin D.

A five-month-old boy with Omenn syndrome successfully recovered after a stem cell transplant with reduced intensity conditioning.

BMP4-related anomalies can cause a wide range of eye, brain, and hand/foot problems, and new cases show this variability.

Hormonal therapies are safe and effective for treating acne in female adolescents, with specific treatments for those with endocrine disorders.

Hirsutism, excessive hair growth in women, is often caused by PCOS and can be managed with medication and personalized treatment plans.

A man with hypoparathyroidism had other health issues that led to a diagnosis of a rare autoimmune disorder, APS-1.

Hutchinson-Gilford Progeria Syndrome is a rare genetic disorder caused by a specific gene mutation, characterized by aging symptoms and managed by monitoring heart health and using low-dose aspirin.

Squarticles, tiny particles made from sebum-derived lipids, can effectively deliver minoxidil, a hair growth drug, directly to hair follicles and skin cells, with less skin penetration and more tolerability.

Severe acne in a young girl may indicate underlying hormonal issues.