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A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

Matriptase is crucial for keeping epithelial tissues healthy and functioning properly.

The pandemic changed how often certain skin conditions were diagnosed.

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

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

The document emphasizes the importance of correctly identifying and classifying genetic hair disorders to help diagnose related health conditions.

Darier-White disease causes skin and nail issues, starts around age 20, worsens until 40-50, and has poor treatment options.

A cross-bred lamb with severe skin and movement issues had ichthyosis fetalis but normal vitamin A levels.

Bovines can have rare inherited skin diseases with specific symptoms like hair loss, fragile skin, and abnormal porphyrin buildup.

Many alpacas have skin diseases, with bacterial infections being the most common.

A 15-year-old with KID syndrome developed a rare skin condition called PEHFN.

Isotretinoin is highly effective in treating severe acne, rosacea, and gram-negative folliculitis.

A new mutation in the Connexin 26 gene was found in a patient with KID syndrome, expanding the known disorders linked to this gene.

sPLA2-X is crucial for normal hair growth and follicle health.

Knocking out certain genes in mice helps understand skin and hair growth problems.

New genetic mutations linked to rare skin disorders were found in three newborns.

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

A man developed a rare skin condition after a hair transplant surgery.

Some scalp sores are linked to different inherited skin conditions.

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

A baby from an Indian family had a rare genetic disorder causing no scalp or body hair due to a specific gene deletion.

A rare skin disorder, nevus comedonicus, can appear on one side of the body following Blaschko's lines.

HIV can cause unusual and severe skin problems that are hard to treat.

People with HIV and low T cell counts have more hair and scalp problems.

Symmetrical Acrokeratoderma (SAK) may be a unique skin condition in China, lacking specific treatment and needing long-term monitoring.

Most HIV patients develop skin symptoms that can indicate the stage of their disease.

The document concludes that early diagnosis and treatment are crucial for managing rare hair loss disorders and that more research is needed to improve treatment strategies.

The woman has a rare skin condition called follicular Dowling-Degos disease, which has limited treatment options.

Dogs with dermatomyositis, especially Collies and Shetland Sheepdogs, need better treatments for their skin and muscle inflammation.

Dermatological conditions are complex and treatments often have mixed results.