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A woman's total hair loss from hepatitis C treatment grew back after stopping the medication.

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

Mutations in the desmoplakin gene can cause hair problems and deadly heart disease.

A single amino acid change in the vitamin D receptor can disrupt its function and lead to hair loss.

Obese and non-obese women with PCOS have higher heart risk markers, especially if they are obese.

An 8-year-old boy with Recklinghausen's Disease shows various symptoms and is from a family with close genetic ties.

The document reports a rare case of ECCL with a new association with optic disc colobomas.

Women with PCOS often have irregular periods, a higher chance of infertility and miscarriages, and may improve fertility with lifestyle changes and treatment.

A nine-year-old girl with muscle weakness and total hair loss improved with specific treatments.

Iron deficiency causes hair loss by affecting hair differentiation and cycling.

The P133R mutation in AKR1D1 enzyme causes harmful bile acid buildup, explaining related health issues.

Siblings with signs of virilization should be tested for non-classical congenital adrenal hyperplasia, which does not affect adult height but may impact fertility and well-being if untreated.

A 38-year-old man was diagnosed late with Kearns-Sayre syndrome after being wrongly treated for epilepsy.

CCCA can affect both genders and all ages, and it has a genetic component.

Alopecia can be reversed with timely steroid treatment in VKH and SO diseases.

A boy's scalp infection, usually found on the body, was effectively treated with antifungal cream.

The mK6irs1/Krt2-6g gene likely causes wavy hair in mice.

Korean women with female pattern hair loss have higher levels of ferritin, testosterone, and vitamin D than average.

Women with PCOS may have a higher risk of severe COVID-19 due to hormonal imbalances and vitamin D deficiency.

NAFLD in PCOS patients is linked to early kidney problems.

Low dose valproic acid treatment caused hair loss in a young patient.

Calcitriol-resistant rickets is an inherited disorder that affects hair growth and causes hair loss.

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.

Early detection of specific VDR mutations is crucial for effective treatment and better dental outcomes in children with hereditary vitamin D–resistant rickets.

α-parvin is necessary for skin and hair growth and for the correct orientation of skin cells.

Mild changes in bone markers relate to TCM syndromes in CKD-MBD patients.

APKH in young males may signal early hair loss and needs early attention.

Trichoscopy is effective for diagnosing scalp ACC in darker skin tones.

A man's unusual scalp folds caused by a skin condition were treated with surgery and remained unchanged two years later.

Early recognition and treatment of VATS in transplant patients improve outcomes.