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A gene variant in KRT71 causes the curly fur in Selkirk Rex cats.

The document suggests using standardized methods to track and measure hair loss in alopecia areata, including patient self-assessment and a 50% improvement in specific scores as a treatment goal.

AGA more common in men, increases with age, linked to family history, hypertension, dyslipidemia, and smoking.

A male with aromatase deficiency improved bone health with estradiol treatment.

Losing eyelashes or eyebrows can be a sign of many different health problems and needs a careful approach to treat effectively.

KFSD is a genetic disorder causing hair loss and skin issues, with no effective treatment.

SACUMAN, a rare condition causing hair loss without clear signs, is often misdiagnosed and needs scalp biopsies for accurate detection.

APS-1 in Italy shows diverse AIRE mutations and various autoimmune issues.

SVF-enhanced adipose transplantation shows potential as a hair loss treatment.

Hair loss in elderly women is often caused by various factors, including hormonal changes after menopause.

Corticosteroids may effectively regrow hair in Alopecia Totalis with manageable side effects.

COVID-19 can cause skin issues like chilblains and rashes, which may help in early detection, especially in patients without other symptoms.

Patients with GATA2 deficiency show early skin symptoms that help diagnose the condition.

Daughters of women with PCOS generally experience normal puberty but may have more body hair and different body fat distribution.

Female donor to male recipient sex mismatch and positive ACA-IgG are key risk factors for vitiligo and alopecia areata in chronic GvHD patients.

Behavior therapy and medications, especially clomipramine, can help reduce hair pulling in people with trichotillomania.

The study found no common cause for a girl's crystalline cataract and uncombable hair, suggesting their co-occurrence might be coincidental.

Genetic variants linked to ten skin diseases were found, showing both immune and non-immune factors play a role.

The study found that Central Centrifugal Cicatricial Alopecia mainly affects middle-aged African descent women, is linked to certain hair care practices and genetics, and often goes undiagnosed for years.

Most new moms had their hair grow back within 4-6 months after childbirth, and hair loss is likely due to hormonal changes.

A boy with chromosome 13q deletion syndrome developed eye cancer, a woman with breast cancer lost vision due to a rare side-effect of her treatment, a man's vision worsened after using a hair loss drug, and two rare disorders were discussed. Optical Coherence Tomography is useful for diagnosing and monitoring these conditions.

NBCCS and BFHS might be the same syndrome, helping better identify and manage cases.

Both genetic and lifestyle factors significantly affect female hair loss.

Newborn skin is uniquely prepared to adapt to new environments compared to adult skin.

Hair loss from cancer treatment is very distressing for women due to its impact on self-image and social stigma.

Eye exams are crucial for kids with 13q deletion syndrome, tamoxifen can cause vision loss, Propecia may lead to cataracts, Lipoid Proteinosis causes skin bumps, and OCT is useful for diagnosing macular diseases.

A rare ITGB6 gene variant causes intellectual disability, hair loss, and dental issues.

CCCA is a common scarring hair loss in African descent women, possibly linked to genetics, hair care practices, and health issues like diabetes.

The study concluded that testing hormone levels after stimulation is not reliable for identifying carriers of 21-hydroxylase deficiency; genetic testing is necessary.

Genes related to pigmentation, body rhythms, and behavior change during hares' seasonal coat color transition, with a common genetic mechanism in two hare species.