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EZH2 levels decrease as fetuses develop and are higher in adult skin, which may affect skin growth and repair.

A young Saudi girl with uncontrolled type 1 diabetes and hypothyroidism had two rare conditions, Mauriac syndrome and Van Wyk–Grumbach syndrome.

Trichoscopy is crucial for diagnosing and assessing alopecia areata in children.

Hair greying is seen as a sign of aging; temporary fixes like hair dye are used, but a balanced diet and hair care can help manage it.

Getting insurance to cover the hair loss treatment tofacitinib is hard because it's not officially approved for that use.

Tofacitinib helps improve skin conditions in people with Down syndrome, especially alopecia areata.

Penile strangulation from hair can cause severe harm but can be treated if caught early.

A multi-tiered treatment approach is crucial for managing hidradenitis suppurativa in patients with intellectual and developmental disabilities.

The model accurately predicts age from saliva and buccal cells for forensic use.

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

Reductive stress messes up collagen balance and alters cell signaling in human skin cells, which could help treat certain skin diseases.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

Young adults who had liver disease as children often experience significant health problems and frequently need transplants.

Experts recommend personalized treatment plans for best outcomes in managing Alopecia Areata.

A certain mutation in the fetal alpha 5-reductase gene is linked to a higher risk of late miscarriage.

Paternal drug exposure can harm fertility, pregnancy outcomes, and offspring health, with specific drugs linked to various reproductive issues.

Identical twins had different symptoms because one had more cells with an extra chromosome fragment in different tissues.

A girl with lupus and trisomy X has a higher risk of bone problems like avascular necrosis and osteoporosis.

Long-COVID has diverse, long-term health impacts, especially in young people.

Mast cells play a significant role in hair loss conditions like male pattern hair loss and alopecia areata.

The four main causes of hair loss in children are fungal infections, pulling out hair, autoimmune hair loss, and stress-related hair shedding.

A genetic duplication on chromosome 5 was linked to a woman's unique combination of medical conditions.

The document reports unique growth lines in a child after Stevens-Johnson syndrome, skin reaction from parsnips and sun in a girl, and itchy skin with xanthomas in a boy with Alagille syndrome.

The document says that treating the root cause of hair follicle damage is crucial to prevent permanent hair loss, and treatment options vary.

Understanding normal hair growth and loss in children is key to diagnosing and treating hair disorders.

The TCL1 transgenic mouse model is useful for understanding human B-cell leukemia and testing new treatments.

Abnormal scalp whorls can indicate brain development issues but may also be seen in neurologically normal people.

VDUP1 is found in skin and hair follicles, interacts with sciellin, and may help regulate skin cell differentiation.

The conclusion is that young women with excessive hair growth should be quickly tested for hormonal issues and treated to improve their social well-being.

A woman with acne and baldness was found to have a rare ovarian condition but successfully had a child through fertility treatment.