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A patient with steroid sulfatase deficiency had a unique hair pattern and a brain malformation not previously linked to the condition.

A woman with childhood growth hormone deficiency had multiple hormone deficiencies and developed serious lung and kidney problems later in life.

A patient with congenital erythropoietic porphyria showed eye issues due to porphyrin buildup.

The patient likely has Chrousos syndrome, a rare condition causing insensitivity to glucocorticoids, requiring high-dose dexamethasone treatment.

Human hair follicles have a unique way of using energy and might use the Cori cycle; blocking CCR5 could help treat hair loss.

Patients with chronic graft-versus-host disease often have skin problems like vitiligo and alopecia areata.

Pegvaliase effectively reduces blood phenylalanine levels in most PKU patients, but requires personalized plans and good communication to manage side effects.

A man lost all his hair as a rare side effect after hepatitis C treatment.

The woman had a genetic condition causing high cortisol and androgen levels, treatable with dexamethasone.

High insulin levels are more common and a better predictor of carbohydrate issues in women with PCOS than glucose tolerance tests.

Integrin β1 is crucial for liver structure and function, preventing fibrosis.

Collagenous gastritis is a rare condition causing chronic diarrhea and weight loss, often misdiagnosed due to nonspecific symptoms.

A rare ovarian tumor that produced testosterone caused a blood clot in the lungs and increased red blood cells in a woman.

Dexamethasone can cause diabetes in rats, and Annona muricata bark extract may help lower blood sugar.

Women with PCOS are more likely to have fatty liver disease and worse metabolic health.

Alloxan diabetes, methylthiouracil, cortisone, and adrenaline affect how white mice hair follicles use glucose and cystine and their cell division.

Sorafenib often causes mucositis, hand-foot syndrome, rash, alopecia, diarrhea, and fatigue.

JAK inhibitors can be safely used in alopecia areata patients with latent hepatitis B or tuberculosis, with proper monitoring.

Chinese women with PCOS and a BMI of 24 or higher should be screened for fatty liver disease.

Some women with excess hair growth have a hormone condition that can't be diagnosed by blood or urine tests alone.

A teenage girl had both a rare ovarian tumor and a severe form of polycystic ovarian syndrome.

Anti-epileptic drugs may cause visual and hair side effects due to enzyme inhibition, especially in genetically predisposed individuals.

EtG levels in hair decrease significantly after one month of alcohol abstinence.

A 5-year-old girl with a rare genetic disorder, lipoid proteinosis, showed reduced new lesions but persistent scars after avoiding skin trauma.

There's no strong link between Alopecia Areata, a hair loss condition, and fatty liver, but more research is needed.

The GH-IGF-I axis is likely involved in the hormonal imbalances seen in non-obese women with functional hyperandrogenism.

A woman developed white patches on her skin and curly hair after hepatitis C treatment, likely due to the medication interferon alpha.

Insulin-dependent diabetes alters hair's molecular structure, making it useful for studying diabetes effects.

An over-the-counter vitamin/mineral supplement improved hair loss and blood sugar control in a woman with non-classic 11-hydroxylase deficiency.

Triple H syndrome exists and can vary in symptoms.