Search

everythinglearnresearchcommunity

for

Search:↓

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

Acne in dark skin is influenced by environmental factors and can lead to hyperpigmentation, with various treatment options available.

AMH levels can't reliably tell the difference between LOCAH and all types of PCOS in women with excessive hair growth.

Possible endocrine disorders caused woman's hair loss and obesity in painting.

Hirsutism in young girls can have causes other than PCOS, so diagnoses should be reassessed if treatments don't work.

The case highlights the complexity of diagnosing high testosterone in older women and the need for thorough testing.

Hirsutism in teens is often due to polycystic ovarian syndrome and needs careful assessment and support.

Hirsute women with ovarian-sourced hirsutism are more likely to have irregular periods, with higher BMI and altered hormone ratios.

A specific gene mutation causes Olmsted syndrome.

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

A newborn girl has a rare skin condition with two ulcers on her buttock that are healing on their own.

Hair shaft disorders cause fragile, brittle, and abnormal-looking hair.

The four patients have a unique type of ichthyosis affecting hair follicles.

A child with skin and heart issues had rare genetic mutations affecting skin and heart cell cohesion.

5% topical minoxidil improves hair density and quality in monilethrix patients.

Hair problems can be caused by genetics or the environment, and treatment should focus on the cause and reducing hair damage.

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

THA is a rare condition with no significant clinical consequences if thyroid function is normal.

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.

The document concludes that early diagnosis and a comprehensive treatment plan are crucial for managing hair loss in children, with a focus on both medical and psychological support.

A patient with Ivemark syndrome developed mixed type vitiligo after a hepatitis C infection, showing different treatment responses and immune cell involvement in the skin.

A man had four testicles, two of which were outside the scrotum and looked like fatty lumps.

Early treatment of children's hair loss, which can be caused by various factors, is important due to its emotional impact.

ECCL should be considered in patients with specific skin and eye lesions.

Mutations in the KRT85 gene cause hair and nail problems.

A boy with Sjogren-Larsson syndrome has skin and muscle symptoms due to a specific enzyme deficiency.

Children with short anagen syndrome usually see their hair condition improve as they get older.

Testosterone therapy improved physical and social health in a male with 49,XXXXY syndrome.

The document reports a unique case of woolly hair with a combination of conditions not previously seen together.

The document concludes that an inherited nail condition often improves on its own, and spironolactone effectively treats acne in women.