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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."

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

People with Epidermolysis bullosa have many health problems including poor oral health, which is often neglected due to other medical issues.

Skin problems can be caused or worsened by physical forces and pressure on the skin.

Scientists created stem cells that can grow hair and skin.

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

Epidermal stem cells could lead to new treatments for skin and hair disorders.

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.

The skin is the largest organ, protecting the body, regulating temperature, and producing hormones.

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

Epidermolysis bullosa is a genetic disease causing fragile skin and blisters in both animals and humans.

A new therapy for a skin blistering condition has not been developed yet.

New treatments and diagnostic methods for various animal skin conditions showed promising results.

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

New treatments targeting specific genes show promise for treating keratin disorders.

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

Genetic research has advanced our understanding of skin diseases, but complex conditions require an integrative approach for deeper insight.

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

The new protocol using Cellutome™ and RCM safely assesses wound healing in detail.

Fetuin A, Anigozanthos Flavidus extract, and Ovol2 affect wound healing and skin regeneration.

Keratin mutations cause skin diseases and could lead to new treatments.

Environmental factors can cause mutations in skin proteins, leading to skin disorders.

Certain mutations in a hair growth-related gene cause a type of genetic hair loss.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

The document suggests a possible link between FAM111B gene mutations and increased cancer risk, particularly pancreatic cancer.

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

Most hair loss in children is caused by a few common conditions and is easy to diagnose, but rare types require careful evaluation.

The document concludes that various childhood hair and nail disorders exist, some may improve on their own, and advances in genetics and immunology could enhance treatment and counseling.

The document reviews various hair and nail disorders, their causes, and treatments, emphasizing the need for proper diagnosis and the link between nail changes and systemic diseases.

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