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Itch is a common symptom in patients with chronic venous insufficiency, often accompanied by burning and pain.

Diphencyprone treatment protocols could be simplified as no harm occurred despite not fully following them.

Itch is a common symptom in patients with chronic venous insufficiency, often worsening with standing or sitting and occurring mostly in the evening or at night.

Mycophenolate mofetil improved skin condition in a man with nephrogenic fibrosing dermopathy.

More research is needed on the health effects of hormone therapy for transgender and nonbinary people.

Skin can produce blood cells, often due to disease, which might lead to new treatments for skin and blood conditions.

Testosterone replacement is recommended for men with low testosterone levels and symptoms of hypogonadism.

Genomic profiling for myeloid cancers can find important inherited mutations, but it's challenging when these mutations aren't related to the patient's symptoms.

Testosterone therapy helps boys with hormone deficiencies develop normal male characteristics and grow properly.

MED1 is essential for normal hair growth and maintaining hair follicle stem cells.

The balance of thiol-disulfide in women with hair loss is affected but not damaged.

Melanocytes are important for normal body functions and have potential uses in regenerative medicine and disease treatment.

More research is needed to understand how testosterone is maintained in adult males.

Maintaining DNA health in stem cells is key to preventing aging and tissue breakdown.

High doses of certain vitamins can cause serious side effects and health risks.

Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

Early diagnosis and individualized treatment improve outcomes for Congenital Adrenal Hyperplasia.

Congenital Adrenal Hyperplasia is a genetic disorder with two forms, causing symptoms like early puberty and severe acne, but can be identified through screening and treated with glucocorticoids.

The document concludes that proper diagnosis and a multidisciplinary approach are crucial for managing Congenital Adrenal Hyperplasia effectively.

The document concludes that early diagnosis and treatment of Congenital Adrenal Hyperplasia are crucial for preventing serious health issues and improving patient outcomes.

Mutations in the DSG4 gene can cause a rare hair disorder similar to monilethrix.

European guidelines recommend regular eye and ear exams, skin care, vitamin D supplements, and cautious use of medications for managing congenital ichthyoses.

Some children are born with unusually short, fine hair because their hair growth phase is short, but this often gets better by itself during puberty.

Some hair loss disorders are caused by genetic mutations affecting hair growth.

The surgery for severe congenital ptosis in children is safe and effective, with good long-term results.

Minoxidil use during pregnancy can cause excessive hair growth and multiple birth defects in the baby.

Congenital Triangular Alopecia is a rare, non-scarring hair loss that can be surgically treated in females for cosmetic reasons.

Congenital alopecia in domestic animals is rare and involves abnormal hair follicle development, needing better understanding and classification.

Some babies are born with alopecia areata, and a treatment with clobetasol propionate can regrow hair in half of the cases.