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Researchers found a new mutation in the FERMT1 gene in a Spanish family with Kindler syndrome.

Genetic testing confirmed a rare skin disorder in a young girl, which improved with zinc supplementation.

The study concluded that PKP1 is essential for skin integrity and hair growth, and its dysfunction causes the symptoms of ectodermal dysplasia/skin fragility syndrome.

Understanding skin structure and development helps diagnose and treat skin disorders.

Wnt/β-catenin signaling is important for keeping skin cell attachment structures stable.

Hemp is a promising ingredient for skin products due to its healing and soothing properties.

Combining skin tissue pathology with genetics has greatly improved the diagnosis and understanding of certain skin diseases.

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

A child with skin and heart issues had rare genetic mutations affecting skin and heart cell cohesion.

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

The document concludes that eyelash trichomegaly, which is the abnormal growth of eyelashes, can be present from birth, caused by diseases, or result from certain medications.

Understanding fetal skin development helps diagnose congenital skin diseases.

The document suggests that certain protein deficiencies and scalp blistering in Epidermolysis Bullosa may cause hair loss.

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

Changes in keratin affect skin health and can lead to skin disorders like blistering diseases and psoriasis.

Three new types of a skin blistering disease were found, caused by specific gene mutations.

Pili torti is a rare condition where hair is twisted and breaks easily, often linked to genetic disorders or other health issues.

Mice with a mutated Dsg3 gene showed severe symptoms but not the typical blistering of pemphigus vulgaris.

UVB is good for a skin condition in Asian kids, a lotion works for head lice, a drug helps with a skin blistering disorder, a foam reduces itchiness in skin inflammation, birthmarks can be more widespread, and criteria for a neurocutaneous disorder were agreed upon.

A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

Early and personalized treatment for hair loss in young people is crucial to prevent permanent damage and should include psychological support.

The document says that treating the root cause of hair follicle damage is crucial to prevent permanent hair loss, and treatment options vary.

Liquid nitrogen spray caused a temporary, harmless swelling under the skin in an elderly woman.

Men with a certain type of hair loss often use facial moisturizers, and a specific antibiotic treatment may help another hair condition.

Researchers found a genetic link for hereditary hair loss but need more analysis to identify the exact gene.

Skin healing from blisters can delay hair growth as stem cells focus on repairing skin over developing hair.

The document concludes that permanent hair loss conditions are complex, require early specific treatments, and "secondary permanent alopecias" might be a more accurate term than "secondary cicatricial alopecia."

Skin symptoms are important for diagnosing infections in children.

The document concludes that inherited epidermolysis bullosa is a challenging genetic condition requiring multidisciplinary care and new treatments.

Genetic defects and UV radiation cause skin damage and aging.