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Trichotillomania is a challenging-to-treat impulse-control disorder where individuals pull out their hair, more common in females, with some treatments showing benefits.

Researchers found a new ABCD1 gene mutation linked to a rare brain and nerve disorder with unusual brain changes.

Hair loss in postmenopausal women due to ovarian hyperthecosis is rare, but removing the ovaries can significantly improve the condition.

Ovarian Hyperthecosis caused hypersexuality in an older woman and was successfully treated with surgery.

Teriflunomide is effective and generally safe for treating relapsing-remitting multiple sclerosis.

A woman's hair loss and other symptoms were due to a rare hormone deficiency treatable with steroids.

A baby had a rare condition with abnormal blood vessels in the brain and unusual skin and hair growth, possibly a new syndrome.

A comprehensive approach to educating patients and managing side effects is crucial for improving adherence to multiple sclerosis treatments and patient quality of life.

A man developed neurological issues from SARS-CoV-2 without severe breathing problems, worsening to death.

CT scans can find serious prostate cancer even when PSA levels are low.

Finasteride, a hair loss medication, may be linked to stroke in young men.

Multi-omics techniques help understand the molecular causes of androgenetic alopecia.

Regenerative pharmacology, which combines drugs with regenerative medicine, shows promise for repairing damaged body parts and needs more interdisciplinary research.

Taking biotin can lead to incorrect low results in free testosterone tests.

RCM and OCT are effective for diagnosing and monitoring hair-related skin diseases but lack standardized protocols and need more research.

A heterozygous mutation in HTRA1 can cause severe CARASIL symptoms.

Teriflunomide is an effective and safe first-line oral treatment for relapsing multiple sclerosis.

Hair transplant surgery may cause alopecia areata, a new possible complication.

Careful management of chronic hyponatremia is crucial to prevent severe neurological issues.

UVB is good for a skin condition in Asian kids, a lotion works for head lice, a drug helps with a skin blistering disorder, a foam reduces itchiness in skin inflammation, birthmarks can be more widespread, and criteria for a neurocutaneous disorder were agreed upon.

A patient with a rare disease had a unique genetic mutation linked to their symptoms.

The document concludes that early diagnosis of Balint's syndrome is crucial for effective treatment and that understanding drug interactions, like between ritonavir and statins, is important for patient care.

Severe sarcoidosis often requires long-term systemic corticosteroids and multidisciplinary care, with most patients improving but some experiencing persistent symptoms or complications.

People with Alopecia Areata often have thyroid problems like Hashimoto thyroiditis and hypothyroidism.

Ethnic Indian women with PCOS often have early symptoms, delayed diagnosis, and need better information and support for treatment and lifestyle management.

Vitamin B12 deficiency can rarely cause excessive daytime sleepiness.

The article suggests managing interferon beta therapy side effects in MS with dose adjustments, medications, and patient education.

A 13-year-old with 46 XY DSD had ambiguous genitalia due to incomplete masculinization.

Children and adults with Cushing's disease show different symptoms and males have more severe cases; surgery outcomes can be predicted by certain factors.

Early recognition and treatment of severe SLE symptoms can improve outcomes.