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A patient with a rare hair condition and skin disorder showed hair improvement after treatment.

The p.P25L mutation in the KRT5 gene causes a rare skin condition that worsens over time and may lead to hair loss starting in young adulthood.

Three specific genetic variants cause severe skin issues in children with EBS, highlighting the need for early genetic screening.

Skin cells from people with Epidermolysis Bullosa Simplex have abnormally placed and less active mitochondria.

Alopecia in patients with epidermolysis bullosa varies in severity and is often caused by skin blistering or trauma.

Epidermolysis bullosa simplex causes easily blistered skin due to faulty skin cell proteins, leading to new treatment ideas.

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

Hair loss can indicate or worsen with systemic diseases, and treating the underlying condition is important.

Alopecia Areata causes significant structural and compositional changes in hair.

Understanding keratinization is crucial for treating skin conditions like ichthyoses and psoriasis.

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

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

A 37-year-old male with severe skin and internal issues has a rare inherited skin condition called dystrophic epidermolysis bullosa.

The document is a detailed medical reference on skin and genetic disorders.

Skin changes throughout life, from development before birth to aging effects like wrinkles, influenced by both genetics and environment.

The document explains hair and nail biology, common hair loss conditions and treatments, oral and genital skin diseases, and the risks and treatments associated with squamous cell carcinoma.

ALA-PDT is effective and safe for chronic X-ray dermatitis, providing complete or partial remission.

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

A 15-year-old girl has a skin condition causing blisters on her feet, likely inherited from her family.

Different botulinum toxin products and concentrations can effectively reduce sweating, itching, bladder pressure, hair loss, and muscle spasms.

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

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

Mothers have more hair proteins than their children, with age-related differences in protein patterns, and some proteins in hair could indicate early childhood development.

Keratin protein production in cells is controlled by a complex system that changes with cell type, health, and conditions like injury or cancer.

A faulty KLHL24 gene leads to hair loss by damaging hair follicle stem cells.

Hair proteins in preschool children and their mothers could indicate developmental changes and health status.

Loss of keratin K2 causes skin problems and inflammation.

Botulinum Neurotoxin-A can treat acne, oily skin, rosacea, hair loss, prevent scars, relieve nerve pain, reduce excessive sweating, and manage psoriasis, but more trials are needed to confirm its effectiveness.

The specific skin disease variant p.(Arg2000Trp) in plectin can cause a wide range of symptoms, which should be considered when diagnosing patients.

Cutaneous gene therapy could become a viable treatment for skin and hair disorders with improved vector development and gene expression control.