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Hidradenitis suppurativa is a chronic skin condition more common in women, linked to genetics and lifestyle factors, and associated with various other health issues.

Effective acne treatment varies by type, with topical and oral medications showing strong evidence, and patient education and support are crucial.

The document reviews various hair and nail disorders, their causes, and treatments, emphasizing the need for proper diagnosis and the link between nail changes and systemic diseases.

Accidentally eating a topical steroid may rarely cause acute generalized pustular psoriasis.

Treat hair loss with medicine, continue indefinitely.

Keratosis pilaris is a common skin condition where hair follicles get clogged with keratin, mostly on the arms and thighs.

Early diagnosis and treatment with Leuprolide are key for children with precocious puberty.

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.

A certain gene variation is linked to a higher risk of polycystic ovarian syndrome in South Indian women.

Type 2 diabetes in youth is increasing, with high treatment failure rates and more severe than Type 1; certain drugs can lower lipid levels effectively with varying side effects, and apples may benefit heart health like statins but with fewer side effects.

UVB is good for a skin condition in Asian kids, a lotion works for head lice, a drug helps with a skin blistering disorder, a foam reduces itchiness in skin inflammation, birthmarks can be more widespread, and criteria for a neurocutaneous disorder were agreed upon.

The document concludes that Syndromes of Severe Insulin Resistance are rare disorders with limited treatment options.

The document concludes that understanding hair biology is key to treating hair disorders, with gene therapy showing potential as a future treatment.

Finasteride effectively treated hidradenitis suppurativa.

Kerascalp hair serum was found to be safe and effective in improving hair growth and strength in people with mild to moderate hair loss.

A specific gene mutation causes Olmsted syndrome.

Substance P may play a role in the inflammation seen in keratosis follicularis spinulosa decalvans.

A rare ear-area hair cyst was successfully removed from a 10-year-old boy.

People with Birt-Hogg-Dubé syndrome often have lung problems and delayed diagnosis, and better recognition of CT scan signs could improve diagnosis and management.

Janus kinase inhibitors show promise in treating alopecia areata but need better topical formulations.

Swiss experts recommend specific guidelines for diagnosing and treating hidradenitis suppurativa to improve patient care.

Keratosis pilaris is often linked to genetic mutations and causes skin and hair abnormalities, regardless of those mutations.

Genetics and nutritional deficiencies are key factors in premature graying of hair.

Melasma's causes include genetics, sun exposure, hormones, and oxidative stress, and understanding these can help create better treatments.

Two siblings with a genetic mutation had a form of rickets that doesn't respond to vitamin D.

A 25-year-old man with multiple skin tumors was successfully treated with acitretin and methotrexate.

Shock can be an early sign of Autoimmune Polyendocrine Syndrome Type II.

Brothers of women with PCOS tend to have higher levels of a hormone called DHEAS, indicating a possible genetic link.

The conclusion is that genetic testing is important for diagnosing and treating various genetic hair disorders.

Different causes of beard hair loss have various treatments, including medications, lifestyle changes, and procedures to stimulate hair growth.