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A protein called PCBP2 controls the production of a hair growth protein by interacting with its genetic message and is linked to hair loss when this control is disrupted.

A mother and daughter have a rare genetic hair loss disorder with no effective treatment.

Mother and son diagnosed with a rare genetic hair loss condition with no effective treatment.

Genetic mutations cause various hair diseases, and whole genome sequencing may reveal more about these conditions.

Ayurveda's descriptions of genetic disorders align with modern genetic understanding.

The document concludes that understanding the genes and pathways involved in hair growth is crucial for developing treatments for hair diseases.

Some children are born with unusually short, fine hair because their hair growth phase is short, but this often gets better by itself during puberty.

Mutations in the DSG4 gene can cause a rare hair disorder similar to monilethrix.

Minoxidil solution applied twice daily improved hair growth in patients with Woolly Hair/Hypotrichosis due to LIPH gene issues, with mild side effects.

A baby from an Indian family had a rare genetic disorder causing no scalp or body hair due to a specific gene deletion.

The research found that a specific gene mutation causes fewer hair follicles and disrupted hair growth cycles, leading to thin and short hair in people with Hypotrichosis with Juvenile Macular Dystrophy.

A new genetic change in the DSC3 gene is linked to a rare condition causing hair loss and skin blisters in a child.

A boy's skin fragility and sparse hair were caused by a genetic mutation affecting skin cell adhesion.

A hair growth ointment improved hair length in a family with a genetic hair growth condition.

Some horses lose hair without inflammation or itching due to various conditions, and while mainly a cosmetic issue, diagnosis requires examination and biopsies, and breeding is not advised if it's hereditary.

Hair loss in Clouston's syndrome improved with minoxidil and tretinoin treatment.

The document concludes that hair loss in cats is caused by various factors, including allergies, mites, infections, and hormonal issues, with treatments varying accordingly.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

The document explains how to identify different hair problems using a microscope.

New gene identification techniques have improved the understanding and classification of inherited hair disorders.

The article explains the genetic causes and symptoms of various hair disorders and highlights the need for more research to find treatments.

Genetic mutations can cause hair growth disorders by affecting key genes and signaling pathways.

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

A mutation in the KRT71 gene causes a hair disorder by disrupting hair follicle structure and texture.

The document is a detailed medical reference on skin and genetic disorders.

Most hair loss in children is caused by a few common conditions and is easy to diagnose, but rare types require careful evaluation.

Hair shaft dysplasias are abnormal hair conditions that can be inherited or acquired and may signal other health issues, with limited treatment options available.

The document concludes that various childhood hair and nail disorders exist, some may improve on their own, and advances in genetics and immunology could enhance treatment and counseling.

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

Most hair loss in children is caused by a few common conditions, and it's important to diagnose these properly and support the child's mental health.