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Women with non-classic congenital adrenal hyperplasia have higher risk for heart and metabolic problems.

The document reports a unique case of woolly hair with a combination of conditions not previously seen together.

HOXC13 is essential for hair and nail development by regulating Foxn1.

New therapies are being developed that target integrin pathways to treat various diseases.

A specific gene variant is linked to heart disease, increased heart muscle, curly hair, and thick skin on palms and soles.

Finasteride significantly increases scalp hair and prevents hair loss in young and middle-aged men.

Women with congenital adrenal hyperplasia have lower fertility, but with proper treatment, they can conceive successfully.

Children with classic congenital adrenal hyperplasia have thicker heart fat and more heart and blood vessel risk factors, especially if their condition is not well-controlled.

Patients often experience long-lasting changes to their hair after stem cell transplants.

P-cadherin is important for hair growth and health, and its problems can cause hair and skin disorders.

Nonclassic congenital adrenal hyperplasia is a common genetic disorder that can cause a range of symptoms and requires personalized treatment.

About 2.2% of women with symptoms of high male hormones have a mild form of congenital adrenal hyperplasia, and measuring a specific hormone level can accurately diagnose it.

The definition of Polycystic Ovary Syndrome may change with new research, and careful screening is key for managing the condition.

Scientists now better understand the genetics of hypohidrotic ectodermal dysplasia, leading to more accurate diagnoses and potential new treatments.

New treatments for ichthyosis, like protein replacement and gene therapy, show promise and may become standard care.

Bovines can have rare inherited skin diseases with specific symptoms like hair loss, fragile skin, and abnormal porphyrin buildup.

A gene called Gk5 controls lipid production in the skin and affects hair growth.

Taking riboflavin and eating less lysine can help some people with a specific genetic disorder avoid brain damage.

Children with classic congenital adrenal hyperplasia have thicker heart fat and are at higher risk for heart problems and early atherosclerosis.

Lack of cystatin M/E causes thin hair and dry skin.

The document concludes that proper diagnosis and treatment of hair shaft disorders require understanding their unique causes and avoiding hair-damaging practices.

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.

EGFR and mTOR inhibitors may help manage Olmsted syndrome symptoms.

Premature graying of hair may suggest health issues and currently lacks effective treatments.

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

L-Carnitine-L-tartrate may help hair grow and prevent hair loss.

The document concludes that secondary syphilis cases are increasing and often misdiagnosed, pityriasis rubra pilaris can be distinguished from psoriasis by skin cell features, and different skin layers produce specific components during skin repair.

Genetics, stress, and health issues can cause early hair greying, which affects self-esteem, and there's no cure, only hair dye.

Lysophospholipids like LPA and S1P are important for hair growth, immune responses, and vascular development, and could be targeted for treating diseases.

Hoxc13 gene affects wool length in Gansu alpine fine-wool sheep.