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

The HtrA1L364P mutation causes brain dysfunction and blood vessel damage.

Most adrenal cortex tumors are benign and non-secreting, but proper diagnosis and treatment are important due to the rare possibility of cancer.

FGF5 spliceosomes inhibit rabbit hair growth by affecting gene expression.

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

The meeting highlighted the importance of genetic testing and multidisciplinary approaches in pediatric dermatology.

FoxN1 gene is crucial for proper thymus structure and normal skin appearance.

The conclusion is that proper signaling is crucial for hair growth and development, and errors can lead to cancer or hair loss.

Using neurohormones to control keratin can lead to new skin disease treatments.

Mice with LSS deficiency showed hair loss and cataracts, similar to humans, and can help in understanding and treating this condition.

Inhibiting AP1 in mice skin causes structural changes and weakens the skin barrier.

Longer CAG and GGN repeats increase alopecia risk, but no significant link to post-finasteride syndrome found.

Biotin and acetazolamide improved hair and nail growth, mental function, and reduced headaches in a child with autism.

Certain genetic changes in the LSS gene cause a rare skin and hair condition.

People with Myotonic Dystrophy type 1 are more likely to have certain skin conditions, but not more likely to get skin cancer.

A woman's long-term scalp issues were diagnosed as a rare skin disorder called cutaneous Langerhans cell histiocytosis.

The conclusion is that adult males with muscle weakness and hormonal imbalances should be tested for Kennedy's disease.

Shorter CAG repeats may cause hair and skin issues, while longer ones may link to acne.

Melanoma's complexity requires personalized treatments due to key genetic mutations and tumor-initiating cells.

Hormones and genetics play key roles in male and female baldness, which can affect mental health and may be linked to other health issues.

Testosterone significantly affects sexual desire in both men and women, but its impact on women is more complex and influenced by psychological factors.

The document concludes that a new biosensor can efficiently detect prostate cancer cells and that standardized referrals help find significant cancers effectively.

CEC levels may be a useful marker for predicting prostate cancer progression.

SLICK cattle have better heat tolerance due to specific gene expression and pathway differences.

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

An individual's morning or evening preference can predict changes in their body clock gene expression.

A boy with severe immune deficiency and Epstein-Barr virus died from high-grade B-cell lymphoma.

Rice bran oil extracted by supercritical CO2 is considered non-genotoxic.

Oestrogens are key for bone growth during puberty in both boys and girls.

The study suggests that motor neurons created from stem cells of patients with spinal and bulbar muscular atrophy show signs of the disease, including changes in protein levels and cell functions.