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Ultrasound is a useful, non-invasive tool in dermatology for diagnosing skin conditions and guiding treatments, but it has some limitations.

Frontal fibrosing alopecia is a challenging hair loss condition with no known cause or definitive treatment.

Early and accurate diagnosis of congenital smooth muscle hamartomas is crucial to distinguish them from other conditions.

The HSD3B1 variant increases hair loss risk in overweight women with PCOS.

The patient with severe hirsutism improved after being diagnosed with non-classic congenital adrenal hyperplasia and treated with corticosteroids.

Hedgehog signaling controls hair follicle development and can affect skin cancer growth.

Multiple perifollicular fibromas may actually be unrecognized cases of Birt-Hogg-Dubé syndrome.

South Asian women with PCOS experience more psychological distress and have a poorer quality of life, especially in social relationships, with hirsutism affecting them more than obesity.

Hippocampus sparing whole brain radiation therapy prevents hair loss and preserves cognitive function.

Dogs could be good models for studying human hair growth and hair loss.

Familial dyskeratotic comedones are a rare, benign skin disorder that is hard to treat.

Excessive hair growth can be assessed by history, exam, and blood tests, and treated with medication like dexamethasone, birth control pills, and spironolactone.

Polycystic Ovary Syndrome (PCOS) is common in women with conditions like anovulation, hirsutism, hair loss, and type 2 diabetes, and it can lead to health risks like heart disease, obesity, insulin resistance, and depression. Non-Classic Congenital Adrenal Hyperplasia (NC-CAH) is also discussed.

Women with PCOS have higher levels of certain androgens, which are good at predicting excess hair growth.

Hereditary elliptocytosis causes elongated red blood cells and can lead to mild or no symptoms.

Hair follicle stem cell secretions may help protect brain cells and improve stroke recovery.

Tenofovir is more effective than adefovir for resistant hepatitis B, Fibroscan is good for assessing liver damage, regulatory T cells may help hepatitis C persist, and other insights into liver health and disease were found.

Foxp1 helps control hair stem cell growth and response to stress during hair growth cycles.

Androgens reduce hair growth by affecting cell differentiation and blood vessel formation.

A rare genetic mutation causes Woodhouse-Sakati syndrome symptoms.

Notch1 signaling is impaired in hidradenitis suppurativa, affecting skin and hair cells.

Frontal Fibrosing Alopecia is a hair loss condition mainly affecting postmenopausal women, with unclear causes and various clinical patterns.

Oral minoxidil and growth factors improved hair density and thickness in a girl with hereditary hair loss.

Hirsutism in young girls can have various causes beyond PCOS, so diagnoses should be reconsidered if treatments don't work.

The French Endocrine Society suggests diagnosing PCOS with two of three signs, recommends lifestyle changes and clomiphene for treatment, and calls for more research on certain treatments and tests.

A mutation in the SREBF1 gene causes both hereditary mucoepithelial dysplasia and IFAP syndrome, which are related conditions.

Hidradenitis Suppurativa has genetic links, with certain gene mutations more common in patients and a third of cases having a family history.

Human hair follicle stem cells can safely and effectively help nerve regeneration.

The scaffold helps wounds heal without scars and promotes hair growth.

Finasteride improves hidradenitis suppurativa in children with no adverse effects.