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The conclusion is that formalizing how past decisions influence current health technology assessments could improve the credibility and defense of coverage decisions.

Recent progress has been made in understanding inherited hair and nail disorders.

A man with hypoparathyroidism had other health issues that led to a diagnosis of a rare autoimmune disorder, APS-1.

Antiviral medication valganciclovir may improve skin and hair in Trichodysplasia Spinulosa patients.

The document concludes that careful design of genetic fate mapping experiments is crucial for accurate cell lineage tracing in mice.

Bald thigh syndrome in sighthounds is caused by structural defects in hair shafts due to downregulated genes and proteins.

The document concludes that managing non-classical congenital adrenal hyperplasia in females requires personalized treatment, genetic counseling, and a team of specialists.

The article concludes that hair loss has many causes and treatments, with medication options like finasteride and minoxidil for men, and minoxidil, hormones, or iron for women, while warning against unproven remedies.

Genetic screening for NUDT15 polymorphisms is crucial for patients taking azathioprine, especially in Asians.

The conclusion is that proper evaluation and treatment of hair loss in midlife women is important, considering the emotional impact and potential for various treatments.

Correct testosterone levels for age to treat prostate cancer, using low dose treatments as necessary.

Men with a certain baldness pattern at age 40-50 may have a higher risk of aggressive prostate cancer.

The 2024 guideline updates recommendations for genetic testing, imaging, and sperm retrieval in male infertility.

KRT14 gene variants cause dermatopathia pigmentosa reticularis, affecting nails, teeth, and hair.

The symposium highlighted the skin's role in sensing itch, pain, touch, and pleasure, and discussed new research and techniques for understanding and treating these sensations.

The document discusses new cosmetic dermatology technologies, safety, robotic hair restoration, and upcoming courses on genomics and skin cancer management.

New methods have greatly improved our understanding of stem cell behavior and roles in the body.

A new mutation in the Hairless gene causes hair loss in two Pakistani families.

DNA variants can predict male pattern baldness, with higher risk scores increasing baldness likelihood.

Psoriasis worsens in winter in India due to less sunlight and dry skin, needing personalized treatment.

Combining genetic and physical trait analysis improves diagnosis accuracy for monogenic diabetes.

Intralesional chemotherapy with 5-fluorouracil and methotrexate may worsen keratoacanthoma-type skin cancer in transplant patients.

Genetic research may lead to better ways to predict and treat male-pattern hair loss.

New, safer treatments for children's hair disorders are needed, and better evaluation methods are recommended.

Children's hair loss has many causes and requires careful diagnosis and personalized treatment, including emotional support.

Three specific mutations in the LIPH gene can cause hair loss by damaging the protein's structure and function.

Mice are useful for researching human hair loss and testing treatments, despite some differences between species.

About 15% of adolescent girls in a region of India have Polycystic Ovarian Syndrome, which is more common in those born by cesarean, with wisdom teeth, or with central obesity.

Betamethasone can effectively treat alopecia areata.

Cancer development is like natural selection, involving mutated cells and environmental factors.