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Middle Eastern patients with epidermolysis bullosa show specific genetic mutations linked to different types of the disease.

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

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

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

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

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

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

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

Natural gene therapy shows promise for treating skin disorders like epidermolysis bullosa.

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

The document concludes that detailed clinical descriptions of seven family cases help understand dominant dystrophic epidermolysis bullosa's symptoms and inheritance.

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

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

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.

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

A Chinese male with a new genetic mutation has a skin condition and severe urinary issues, with treatments having mixed success.

Most patients with Tuberous sclerosis had neurological or skin issues, and over half had psychiatric problems.

Yellow dots look different in various hair loss conditions and can help diagnose them.

A man with Klinefelter syndrome had a leg ulcer that didn't heal well, even with treatment.

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."

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

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

Immune cells are essential for early hair and skin development and healing.

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

Older mice healed wounds better but lost more weight and might have weaker immune systems afterward.

Anigozanthos Flavidus flower extract helps regenerate skin and reduce wrinkles.

Ovol2 is important for proper skin healing and hair growth.

Fetuin A may increase collagen production and promote scarring.

The document concludes that an experimental drug may help wound healing in Epidermolysis Bullosa, links Hydroa vacciniforme to EBV, discusses diagnosing hair loss disorders, finds many children with eczema have allergies, reviews the safety of a skin medication in children, notes side effects of a Duchenne's treatment, and identifies a marker for pediatric mastocytosis.

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