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Hair loss linked to prostate enlargement; stress and family history important factors.

Using steroids can increase the risk of heart problems.

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."

WWOX deficiency in mice causes skin and fat tissue problems due to disrupted cell survival signals.

A woman with a rare hormone resistance condition also had missing teeth and hair loss, which might be new symptoms of her genetic disorder.

The conference presented findings on how vitamin D levels, genetic factors, and lifestyle choices like smoking and yoga affect various health conditions and diseases.

New genes and pathways are important for testosterone production and male sexual development.

Genetic mutations can cause hair growth disorders by affecting key genes and signaling pathways.

Hair loss in Androgenetic Alopecia is caused by genetics, aging, and lifestyle, leading to hair follicle shrinkage and related health risks.

Female pattern hair loss has unclear causes, possibly involving genetics, hormones, and environment, and needs better treatments.

Regenerative pharmacology, which combines drugs with regenerative medicine, shows promise for repairing damaged body parts and needs more interdisciplinary research.

Genetic mutations can affect female sexual development, requiring personalized medical care.

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

A patient with Ivemark syndrome developed mixed type vitiligo after a hepatitis C infection, showing different treatment responses and immune cell involvement in the skin.

Bleaching hair damages protein structure, especially keratin, leading to weakened hair.

An 11-year-old child with total hair loss may have a genetic autoimmune disease, and the outlook for hair regrowth is not good.

A mutation in the EDNRA gene causes Oro-Oto-Cardiac syndrome, affecting face and heart development.

K_ATP channel gene mutations are linked to heart diseases, but more research is needed to understand the connection and treatment potential.

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.

Minoxidil was more effective than laser therapy for hair loss, and the report also highlighted the need for more research on PRP for a different hair loss condition, the impact of social media on alopecia views, and a warning on turmeric causing nail discoloration.

Different hair and scalp disorders cause hair loss or excess hair growth, with various treatments available depending on the specific condition.

Diabetes often causes various skin problems and complications.

Diagnosing sex development disorders requires combining medical history, physical exams, imaging, lab tests, and genetic data.

Epidermolytic ichthyosis can be inherited in a semidominant way with mild symptoms in carriers.

A baby was diagnosed with IFAP syndrome due to a new genetic mutation, showing severe skin and developmental issues.

BMP4-related anomalies can cause a wide range of eye, brain, and hand/foot problems, and new cases show this variability.

Cholesterol sulfate buildup due to a genetic mutation disrupts the skin barrier, leading to the scaling skin seen in X-linked ichthyosis.

The document describes skin diseases affecting the outer ear in dogs and cats, their spread to other body parts, and treatment options.

The research found specific genes and proteins that affect how fast chickens' feathers grow, which is not solely determined by traditional inheritance patterns.

An 11-year-old girl with a rare skin disorder also had cornea issues and dry eye, needing careful management.