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Finasteride, often used for hair loss, can potentially cause cataracts.

The document reports three sisters with Woodhouse-Sakati syndrome showing typical symptoms and unusual gynecological anomalies.

A 2-year-old boy had no hair and unusual organ placement, and it's unclear if it's genetic or coincidental.

Multiple eye conditions were studied, highlighting the importance of various imaging methods for diagnosis, the vision side effects of drugs tamoxifen and Propecia, and the usefulness of optical coherence tomography for diagnosing and monitoring macular and retinal diseases.

A girl with a rare syndrome had successful hair loss treatment with no relapse after 4 years.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

Acne is a common skin condition linked to diet, hormones, and genetics, and early treatment can prevent scarring.

Minoxidil solution used on the scalp did not lower blood pressure in patients without hypertension.

A family was found with both Trichorhinophalangeal syndrome and Loose Anagen Syndrome, suggesting a genetic connection.

The flap advancement technique effectively treats severe scalp skin conditions, preserving hair and improving appearance.

Hair follicle sampling is a feasible method to measure FMRP and FMR1 mRNA levels in children.

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

A baby had a unique skin condition with a pale patch and surrounding dark hairs, not linked to other health issues.

Netherton Syndrome is a non-treatable genetic disorder in children causing skin, hair, and allergy issues.

Trichotillomania is a chronic hair-pulling disorder, more common in females, treated with therapy and sometimes medication.

Trichotillomania is more common than previously thought, with increasing diagnosed cases.

Hair mineral analysis might help diagnose diseases early, but standard methods are needed.

The document concludes that early diagnosis and a comprehensive treatment plan are crucial for managing hair loss in children, with a focus on both medical and psychological support.

Chemotherapy in the first trimester of pregnancy is risky, but in the second and third trimesters, it's generally safe with careful drug selection and timing.

Childhood obesity is rising globally due to various factors, and early prevention and healthy lifestyle changes are crucial.

Alopecia areata, a common autoimmune hair loss condition, often runs in families.

The document concludes that the 5 alpha-reductase enzymes are important in steroid metabolism and related to various human diseases, with inhibitors used to treat conditions like male pattern baldness and prostate issues.

Omeprazole effectively treats severe acid reflux in children for short-term use, but long-term safety needs more research.

The WNT signaling pathway is important in many diseases and targeting it could offer new treatments.

The document concludes that understanding hair structure is key to diagnosing hair abnormalities and recommends gentle hair care for management.

New targets for making and using brain-synthesized steroids could lead to better treatments for brain disorders and alcoholism.

The AUTS2 gene is linked to neurological disorders and may affect human brain development and cognition.

Cholesterol sulfate buildup due to a genetic mutation disrupts the skin barrier, leading to the scaling skin seen in X-linked ichthyosis.

Six new genetic regions linked to early hair loss also connect to Parkinson's disease and prostate cancer, possibly leading to new treatments.

Trichoscopy is a useful non-invasive method for diagnosing different hair loss conditions.