Search

everythinglearnresearchcommunity

for

Search:↓

The document concludes that adult mammalian skin contains multiple stem cell populations with specific markers, important for understanding skin regeneration and related conditions.

Abnormal scalp whorls can indicate brain development issues but may also be seen in neurologically normal people.

Mutations in the desmoplakin gene can cause hair problems and deadly heart disease.

A litter of cats had a hair condition similar to a mouse mutation, leading to hair loss and abnormal hair and skin.

The document recommends several books on cosmetic surgery and complementary medicine, highlighting their detailed methods, multidisciplinary approaches, and valuable treatment insights.

The document explains different hair and scalp conditions, including common hair loss after pregnancy or illness, drug-induced hair loss, hereditary excessive hair growth, patterned baldness, autoimmune hair loss, and permanent loss due to skin disease, with generally limited treatment options.

Targeted cancer therapies can cause skin side effects, but activating SOS in the skin may help reduce them.

Uncombable hair syndrome causes frizzy hair and can affect the nervous system, eyes, and ears, often co-occurring with other hair, skin, nail, and teeth conditions, and is linked to three specific gene mutations.

A mutation in the KRT82 gene is significantly associated with Alopecia Areata.

Loss of Msx2 function causes eye development issues similar to Peters anomaly.

The document concludes that Rabson-Mendenhall syndrome requires novel treatments for insulin resistance and emphasizes the importance of dental care in affected patients.

Understanding intermediate filaments helps explain hair health and related diseases.

Hairless protein affects hair follicle structure by regulating the Dlx3 gene.

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

Amenorrhea, or missing periods, is caused by various factors and is treated based on the specific cause.

EGFR inhibitors cause skin issues and hair loss by weakening skin defenses, suggesting antibiotics and targeted treatments can help.

HOXC13 is essential for hair and nail development by regulating Foxn1.

People with primary immunodeficiencies often have frequent, severe, or unusual infections and may need special tests and management strategies.

A new mutation in the XEDAR gene might cause a rare skin condition called hypohidrotic ectodermal dysplasia.

P-cadherin is important for hair growth and health, and its problems can cause hair and skin disorders.

TRPV3 could be a target for treating pain, skin disorders, and hair problems, but more research is needed to create effective drugs.

Both genes and environmental factors like chemicals may contribute to the increase in hypospadias, but the exact causes are still unclear.

Different processes create patterns in skin and things like hair and feathers.

Msx2 and Foxn1 are both crucial for hair growth and health.

Certain genetic variations are linked to increased androgen levels in PCOS, but more research is needed to understand these connections fully.

The document concludes that insulin resistance is key in PCOS development and early treatment is crucial to prevent complications.

Exposure to too much androgen before birth might cause polycystic ovary syndrome later in life.

Humans lost body hair relatively recently in evolution.

Hair, teeth, and mammary glands develop similarly at first but use different genes later.

Mutations in the PTPRQ gene cause significant balance issues in mice due to hair bundle defects in the inner ear.