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A cross-bred lamb with severe skin and movement issues had ichthyosis fetalis but normal vitamin A levels.

Doctors should consider Netherton syndrome in patients with chronic skin and hair issues to avoid misdiagnosis.

A baby with maple syrup urine disease improved from skin problems by adjusting his diet to correct amino acid levels.

A baby from an Indian family had a rare genetic disorder causing no scalp or body hair due to a specific gene deletion.

Genetic testing confirmed a rare skin disorder in a young girl, which improved with zinc supplementation.

An infant with a zinc deficiency skin disorder improved with zinc treatment.

A 5-year-old Akita with a rare skin condition improved significantly after treatment.

A patient with sickle cell trait and low vitamin D might have lupus, a rare combination that needs more attention.

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

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.

Hormones, especially testosterone and DHT, are key for penis development and function, and testosterone therapy may help with erectile dysfunction in those with low levels.

A new TP63 mutation was found in a baby with EEC syndrome, showing the need for TREC testing to check for immune issues.

Vitamin D3 and its receptor are important for hair growth, and understanding receptors could help treat hair graying and skin cancer.

Mimicking growth factors in a topical solution can prolong hair growth phase and reduce hair loss without side effects.

A woman with CHILD syndrome showed skin abnormalities, and the report suggests CHILD nevus and NEVIL might be the same condition, highlighting the need for diagnosis for genetic advice.

A woman's nail separation was likely caused by poor blood flow, and a treatment for similar conditions might help.

Surgery on a baby with a skin disorder improved eyelid position and eye health.

The document concludes that Borrelia afzelii causes a skin condition in France, a gene is linked to hair loss in Caucasian women, and various genetic mutations affect skin diseases.

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

Transverse sections are better for non-scarring hair loss, vertical sections are better for lichen planopilaris, and either method works for other scarring hair loss types.

Mutations in the P2RY5 gene cause hereditary woolly hair.

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

Experts discussed treatments for skin conditions in children, emphasizing hydration, cautious medication use, and early intervention for infections.

TNF family proteins are crucial for the development of skin features like hair, teeth, and mammary glands.

Fat tissue stem cells may help increase hair growth.

Sphynx cats are hairless and Devon Rex cats have curly hair due to specific genetic mutations.

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.

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

A new mutation in the HR gene causes hair loss in a specific family.