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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.

Scientists have found specific genes linked to different hair loss conditions, which could lead to new treatments.

The document concludes that hair loss in cats is caused by various factors, including allergies, mites, infections, and hormonal issues, with treatments varying accordingly.

Children's hair loss can be caused by many factors, including autoimmune diseases, emotional stress, genetics, and infections, with treatment and prognosis varying.

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

Changing the environment around stem cells could help tissue repair, but it's hard to be precise and avoid side effects.

Stem cells are crucial for skin repair and new treatments for chronic wounds.

Scientists created stem cells that can grow hair and skin.

The Foxn1 gene mutation causes hairlessness and immune system issues, and understanding it could lead to hair growth disorder treatments.

Certain groups may need vitamin supplements to improve hair health and prevent other health problems.

Recognizing oral symptoms can help diagnose and treat blood and nutritional diseases early.

No consistent link between genotype and phenotype in 5-α-Reductase type 2 deficiency.

Losing eyelashes or eyebrows can be a sign of many different health problems and needs a careful approach to treat effectively.

Madarosis is the loss of eyelashes and eyebrows due to various health issues and requires thorough examination to diagnose and treat the underlying cause.

Acne is significantly influenced by genetics, and understanding its genetic basis could lead to better, targeted treatments.

Eyebrow loss has many causes and requires accurate diagnosis for proper treatment.

A gene deletion causes the "hairless" trait in Iffa Credo rats.

Systemic diseases can cause hair loss, which is often reversible with treatment.

Most skin diseases in Hajjah, Yemen, were dermatitis, infections, and acne, influenced by local socioeconomic and environmental factors.

Childhood ptosis can vary from a minor cosmetic issue to a serious condition and may signal other health problems.

Hirsutism is too much hair growth in women like the pattern in men, often caused by high male hormones, and can be treated with hormone control and hair removal methods.

The document concludes that hair loss is common and can be treated with medications like minoxidil or surgical options, and it significantly affects people's psychological well-being.

New mutations in the SLC39A4 gene found in twins help understand the genetic cause of acrodermatitis enteropathica.

The document concludes that managing female hyperandrogenism requires a combination of identifying the cause, lifestyle changes, medication, and cosmetic treatments.

The cornified envelope is crucial for skin's barrier function and involves key proteins and genetic factors.

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

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

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

Genetic testing is crucial for diagnosing congenital atrichia, a rare condition causing irreversible hair loss.

The document concludes that the girl's hairlessness is likely inherited from her parents.