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Topical minoxidil and tretinoin improved hair growth in a girl with EDSS1 over two years.

The cat died from a hard-to-treat fungal infection despite various treatments.

European guidelines recommend regular eye and ear exams, skin care, vitamin D supplements, and cautious use of medications for managing congenital ichthyoses.

Steroids, infection management, and nutritional support can significantly improve symptoms of Cronkhite-Canada Syndrome.

The hair disorder was caused by abnormal protein formation, making hair easily damaged.

A family showed a new condition with inherited hair loss and skin changes, possibly due to one genetic disorder.

A 17-year-old with Netherton syndrome has dry, itchy skin, brittle hair, and high IgE levels, treated with antihistamines and emollients.

A 6-year-old girl was diagnosed with a rare hair disorder and started treatment with topical minoxidil.

Cancer treatments can cause various eye problems, so eye doctors should know how to diagnose and treat these early.

Scalp biopsies from dermatomyositis patients show chronic hair loss without scarring, with mucin and blood vessel changes being very common.

A mutation in the HOXC13 gene causes hair and nail problems in a Syrian family.

A man with a rare skin condition and a new gene mutation developed high calcium levels due to his treatment.

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

Trichoscopy can diagnose Netherton syndrome without pulling hairs.

LC-OCT can help identify lupus-related scarring hair loss by spotting unique features.

A missing mK6irs1 gene causes hair loss in mice.

CYLD deficiency in skin tumors disrupts hair follicle cell processes and protein secretion.

Recognizing the "bamboo hair defect" is crucial for diagnosing Netherton's syndrome.

Malassezia in cat skin biopsies may indicate internal cancer.

Topical eyedrops may cause eyelash whitening and skin lightening around the eyes.

Topical ceramide treatment partially improves the skin condition in Jack Russell Terriers with a genetic skin disorder.

Enzyme replacement therapy improved multiple symptoms of homocystinuria in mice.

Accurate diagnosis of EFFC is crucial for effective counseling and cosmetic care.

Dermatophylosis sporadically affects adult sheep in Sertão da Paraíba, causing alopecic and crusty skin lesions.

Keratin mutations may cause scarring alopecia by damaging hair structure.

The treatment for alopecia areata with diphenylcyclopropenone was unsuccessful.

Mite infestations severely harm the health of endangered Amargosa voles.

GABEB is a less severe skin condition caused by a gene mutation affecting collagen, leading to blisters and other symptoms.

Yorkshire Terriers with Colour Dilution Alopecia have reduced melanin and hair structure issues.

A 9-year-old girl has a rare hair disorder causing beaded, sparse hair.