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Hair diversity is influenced by complex genetics and environmental factors, requiring more research for practical solutions.

Different fields of expertise must work together to better understand hair growth and create effective hair loss treatments.

Bald thigh syndrome in sighthounds is caused by structural defects in hair shafts due to downregulated genes and proteins.

The document concludes that understanding hair biology and recognizing hair conditions are crucial for managing and treating hair loss in children.

Trichoscopy is good for diagnosing and monitoring hair and scalp problems in children but needs more research for certain conditions.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

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

Premature balding in some men may be linked to altered hormones, but it's not the male equivalent to polycystic ovary syndrome or metabolic syndrome.

Eyebrow loss has many causes and requires accurate diagnosis for proper treatment.

Over 67 genes linked to ichthyosis help improve diagnosis and treatment.

A 37-year-old male with severe skin and internal issues has a rare inherited skin condition called dystrophic epidermolysis bullosa.

Atopic dermatitis may have genetic causes and can be treated with pharmacologic methods, glycerin creams, and controlling Staphylococcus aureus colonization.

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.

Using cetirizine on the skin and taking vitamin D can help increase hair growth in children with hair loss from ectodermal dysplasia.

Children with trichotillomania often pull hair from their scalp, and parents may not notice; stress can trigger it, and asking detailed questions helps in diagnosis and treatment.

Disrupting the FGF5 gene in rabbits leads to longer hair by extending the hair growth phase.

Benign skin tumors need accurate diagnosis to ensure proper treatment.

Woolly hair is a rare genetic condition with no effective treatments.

Hair shaft disorders are diagnosed through examination and history, with general care and some treatments offering improvement.

The document concludes that unruly hair can be congenital or acquired, often lacks specific treatments, and can be managed with oils and short hairstyles.

Normal hair thickness varies by scalp area and a mix of hair thicknesses is typical in healthy individuals.

A man with Woolly Hair Syndrome had very curly, fragile hair, and doctors used a special scalp examination to diagnose him without invasive tests.

Two siblings have a rare genetic condition causing curly, coarse hair.

A 4-year-old girl had a rare hair disorder affecting only part of her scalp.

Frizzy hair is fragile and can lead to hair loss and damage if not properly cared for.

Two sisters have rare hair disorders causing short, fragile, kinky hair.

A Korean girl developed kinky hair without known cause or effective treatment.

Researchers made a mouse model with curly hair and hair loss by editing a gene.

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

Some congenital hair disorders improve with age and can be managed with treatments like minoxidil, retinoids, supplements, and gentle hair care, but there's no cure.