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UVF-dermoscopy is a useful tool for accurately diagnosing types of alopecia, especially in people with lighter skin.

S100A7 and IL-17 may contribute to inflammation in lichen planopilaris.

Antimalarial agents are effective for LPP, and intralesional steroids are effective for FFA.

Twins had rare skin cysts likely due to genetics.

Check serum ferritin levels and total blood count for women with diffuse hair loss.

Early diagnosis is crucial for treating alopecia effectively.

A possible link exists between minimal change nephrotic syndrome and complete hair loss.

Two boys had a rare skin condition needing to be differentiated from similar disorders, with unclear inheritance due to few cases.

A mutation in the hHb3 gene is linked to the hair disorder monilethrix.

A 6-year-old girl had both monilethrix and trichorrhexis nodosa, causing brittle hair, with minimal improvement from treatment.

The study found that Frontal Fibrosing Alopecia in North-East India mainly affects middle-aged women and is often associated with lichen planus pigmentosus.

Erythromelanosis follicularis faciei can also affect women, though it's rare.

Three Iranian men had reddish-brown facial pigmentation with no effective treatment.

Dermoscopy helped diagnose a rare hair disorder in a 2-year-old boy.

The book is a useful guide for dermatologists studying for their board exam, with clinical images and features of skin diseases.

Autosomal recessive woolly hair is rare and involves tightly coiled hair without other health issues.

Baricitinib successfully regrew hair in an 8-year-old boy with alopecia totalis linked to a KRT74 gene variant.

Obesity can cause various skin problems, with differences in prevalence between males and females.

Trichoscopy is useful for quickly diagnosing different types of hair loss without needing biopsies.

The patient improved with treatment for depilating folliculitis.

Cyclosporine effectively treated a woman's stubborn skin condition.

A rare skin condition causes red, dark, bumpy facial lesions.

A rare skin condition causes red and dark patches on the face and limbs.

Sebaceous glands help protect and maintain healthy skin and hair.

A young girl had a rare neck cyst removed and needs careful monitoring for related health issues.

Mutations in the P2RY5 gene cause autosomal recessive woolly hair.

Mutations in the LSS gene cause hair loss and may affect brain development, with varying severity.

Eruptive vellus hair cysts are rare and often misdiagnosed, requiring biopsy for accurate diagnosis.

Monilethrix, a genetic hair disorder causing fragile hair, affects three generations in a family.