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Isotretinoin can raise CPK levels, so patients need monitoring, especially before surgery.

Kids with early graying hair often have low levels of calcium, ferritin, and vitamin D3.

The EDAR gene mutation leads to thinner and more deformed hair shafts.

A 4-year-old girl was diagnosed with erythrokeratodermia variabilis after other treatments failed.

Treatment with moisturizers improved the skin condition of a girl with a rare genetic skin disorder.

The document concludes that there are various causes and treatments for hair loss, with hair transplantation being a notable option.

The document concludes that understanding hair structure is key to diagnosing hair abnormalities and recommends gentle hair care for management.

The document concludes that better treatments for CCCA are needed and more research is required to understand its causes related to hairstyling and genetics.

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

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

Women with myotonic dystrophy might get diseases related to male hormones because their body tissues are extra sensitive to these hormones.

Cantu syndrome, which causes excessive hair growth and skin issues, is due to a mutation in the ABCC9 gene, and understanding this could help develop new treatments for hair diseases.

Researchers created a model to understand heart aging, highlighting the role of microRNAs and identifying key genes and pathways involved.

A rare skin disorder affecting the face was found in a 28-year-old Saudi man.

Darier-White disease causes skin and nail issues, starts around age 20, worsens until 40-50, and has poor treatment options.

A 5-year-old girl has sparse, dry, and brittle hair but is otherwise healthy.

Acne is linked to inflammation and insulin resistance, and is associated with various syndromes that require different treatments.

Different nail disorders are treated by targeting their specific causes and using appropriate medications or protective measures.

The workshop highlighted the genetic links and psychological impacts of hair loss and skin disorders.

Many adult women experience unexplained excessive hair shedding, often starting before age 40.

Two treatments for male pattern hair loss are minoxidil and finasteride, but they have side effects and may not satisfy everyone.

Premature balding in some men may be linked to altered hormones, but it's not the male equivalent to polycystic ovary syndrome or metabolic syndrome.

Women experience various skin issues at different life stages, requiring careful treatment and awareness.

The document concludes that over 500 genes are linked to hair disorders and this knowledge is important for creating new treatments.

The document concludes that parathyroid diseases have a range of clinical features and outcomes, with some conditions being treatable and others having a high risk of mortality.

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

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

The document concludes that AFA should be considered in patients with acromegaly-like features but normal hormone levels, and more cases need to be identified to understand the condition fully.

The document concludes that a thorough history, physical exam, and specific tests are crucial for diagnosing and managing hair loss effectively.

Using cetirizine on the skin and taking vitamin D can help increase hair growth in children with hair loss from ectodermal dysplasia.