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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.

AIRE-deficient rats developed severe autoimmune disease similar to APECED, useful for testing treatments.

A genetic duplication on chromosome 5 was linked to a woman's unique combination of medical conditions.

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

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

Dermatologists give better information on pathology forms, hypersensitivity vasculitis is a common skin issue, misdiagnoses can occur, and various skin conditions are linked to loss of elastin or genetic factors.

A teenager's hair with alternating white and dark bands, known as Pili annulati, is a genetic condition that is usually harmless and often considered attractive.

Some human genetic markers work for genetic studies in pig-tailed and stump-tailed macaques, which can help in their conservation.

The Itpr3 gene causes a specific hair pattern in mice.

A new gene, JMJD1C, may affect testosterone levels in men.

2011 dermatological research found new skin aging markers, hair loss causes, skin defense mechanisms, and potential for new treatments.

Researchers found two genes that may explain why some Casertana pigs don't have hair.

Certain gene variations might help protect against insulin resistance and glucose intolerance in people with Polycystic Ovary Syndrome.

An 8-year-old girl has a rare, irreversible hair loss condition caused by a genetic mutation.

Different types of long-lasting stem cells are responsible for the growth and upkeep of the mammary gland.

Obesity is linked to various skin problems and may increase the risk of skin cancer.

The document concludes that proper diagnosis and a multidisciplinary approach are crucial for managing Congenital Adrenal Hyperplasia effectively.

A position effect on the TRPS1 gene causes excessive hair growth in humans and mice.

The LRRK2-G2019S mutation in Parkinson's disease has a lifetime penetrance of 25-35%, and finasteride may help reduce symptoms in adult male Tourette syndrome patients.

Some hair loss disorders are caused by genetic mutations affecting hair growth.

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

Genetics play a role in acne, but how exactly they contribute is not fully understood.

Weight loss and metformin don't significantly change vaspin levels in women with PCOS.

The document describes a woman with familial Parkinson's disease due to a genetic mutation, showing severe symptoms and poor response to treatment, and suggests finasteride may help reduce symptoms in Tourette syndrome.

Researchers found a gene mutation responsible for a rare hair loss condition.

A woman's unique dementia was misdiagnosed, a genetic mutation increases Parkinson's risk with age, and finasteride may help with Tourette syndrome.

A complex X chromosome rearrangement can increase the risk of multiple autoimmune diseases.

The Megsin-Cre transgene is a new tool for genetic manipulation in the skin and upper digestive tract.

ATP-dependent chromatin remodeling is crucial for skin development and stem cell function.

Vitiligo is a skin condition causing white spots, more common in women, often starts before age 20, and can affect mental health.