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

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

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

The document explains various skin conditions and their treatments.

The 2015 Hair Research Congress concluded that stem cells, maraviroc, and simvastatin could potentially treat Alopecia Areata, topical minoxidil, finasteride, and steroids could treat Frontal Fibrosing Alopecia, and PTGDR2 antagonists could also treat alopecia. They also found that low-level light therapy could help with hair loss, a robotic device could assist in hair extraction, and nutrition could aid hair growth. They suggested that Alopecia Areata is an inflammatory disorder, not a single disease, indicating a need for personalized treatments.

A child with Olmsted syndrome showed mild improvement in hair and skin issues with treatment.

Certain genetic changes in the LSS gene cause a rare skin and hair condition.

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.

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

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.

Benign skin tumors need accurate diagnosis to ensure proper treatment.

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

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

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

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.

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

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

Four children had unmanageable pale blond hair due to uncombable-hair syndrome.

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

Loose Anagen Syndrome is a hair condition where hairs can be easily pulled out, mainly affecting young girls, and may improve on its own or with treatment.

Loose Anagen Hair Syndrome is found in black-haired Indian children and is often missed, especially in boys.

Loose anagen hair syndrome is caused by structural abnormalities in the hair follicle's inner root sheath.

A Thai boy was diagnosed with a rare hair disorder causing hair thinning and shedding.