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The document explains different types of hair loss, their causes, and treatments, and suggests future research areas.

The man has a genetic skin condition called pachyonychia congenita.

The document concludes that non-endocrine alopecia in pets varies in treatment effectiveness and often has a poor prognosis, especially in cats.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

The review shows how to properly diagnose and treat the loss of eyebrow and eyelash hair.

The document concludes that while there are various treatments for Alopecia Areata, there is no cure, and individualized treatment plans are essential due to varying effectiveness.

Topical PUVA and tacrolimus ointment can effectively and safely treat infant alopecia universalis.

Vitiligo is a skin condition causing white spots, more common in women, often starts before age 20, and can affect mental health.

Acitretin helped improve hand mobility and skin condition in a patient.

The document describes various skin conditions, their features, and treatments but lacks detailed study size information.

WNT10A helps esophageal cancer cells spread and keep renewing themselves.

RSPO1 mutations in certain patients lead to skin cells that don't develop properly and are more likely to become invasive, increasing the risk of skin cancer.

Ellis van Creveld syndrome, a rare genetic disorder, can cause unexpected abnormalities in various body organs, requiring thorough patient evaluations.

The study found that mouse sweat glands develop before birth, mature after birth, and have specific keratin patterns.

Get head MRI for babies with achondroplasia early, use free immunoglobulin light chains to detect certain neurodevelopmental disorders, and video calls work for speech therapy in patients with facial anomalies.

The most common skin problems in Indian children are infections and eczemas.

The document reports unique growth lines in a child after Stevens-Johnson syndrome, skin reaction from parsnips and sun in a girl, and itchy skin with xanthomas in a boy with Alagille syndrome.

MendelVar is a tool that helps identify important genes by combining GWAS data with Mendelian disease information.

Atopic dermatitis may have genetic causes and can be treated with pharmacologic methods, glycerin creams, and controlling Staphylococcus aureus colonization.

Rituximab may be an effective treatment for Cronkhite-Canada syndrome with kidney disease.

The man was diagnosed with Cronkhite-Canada syndrome, a rare disorder with GI polyps, skin issues, hair loss, and nail problems.

A 56-year-old man was diagnosed with Cronkhite-Canada Syndrome after showing symptoms like diarrhea, weight loss, and skin changes.

FOXN1 gene mutations cause a rare, severe immune disease treatable with cell or tissue transplants.

A man with Cronkhite-Canada syndrome had all 20 nails detach but improved with treatment.

First Korean case of Cronkhite-Canada syndrome with colon cancer and serrated adenoma.

The gene Msx2 is crucial for hair follicle regeneration during wound healing.

APS-1 in Italy shows diverse AIRE mutations and various autoimmune issues.

The document concludes that ongoing research using animal models is crucial for better understanding and treating Alopecia Areata.

The document concludes that parathyroid diseases have a range of clinical features and outcomes, with some conditions being treatable and others having a high risk of mortality.

Genetic screening is crucial for accurately diagnosing APS-1 due to its varied symptoms.