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The document concludes that recognizing specific histological features of different nonscarring alopecias is crucial for accurate diagnosis and understanding hair loss progression.

Surgery to fix a broken upper arm bone can sometimes lead to nerve damage.

Passiflora incarnata may help with anxiety but has risks and drug interactions. There's a genetic link between Fragile X Syndrome and Autism Spectrum Disorder. 6.7% of urine cultures showed hospital-acquired urinary tract infections. Children used screens more during COVID-19, causing various health complaints. Autism Spectrum Disorder is often underdiagnosed in females. Dissociative disorders in childhood sexual abuse victims are more common in males. Most pregnant teenagers are not dissatisfied with their body image but worry about weight. Diagnosing tuberculosis after knee surgery is challenging due to non-specific symptoms. Post-COVID-19 syndrome is more common in older, severely affected patients. Psychiatrists should be part of pain management teams due to the psychological aspects of pain.

In the Middle Ages, European noblewomen intentionally removed forehead hair to be fashionable, showing how beauty standards can affect the perception of hair loss.

Best treatment for Frontal Fibrosing Alopecia is 5-alpha-reductase inhibitors and intralesional corticosteroids.

People with cleft lip and palate often have respiratory problems.

Pharmacists play a key role in managing the use of anxiety medications and ensuring patients use them correctly.

Some drugs may reduce prostatitis symptoms short-term with few side effects.

Children's screen time increased during the pandemic, causing various health issues.

Long-COVID has diverse, long-term health impacts, especially in young people.

Basonuclin 2 is vital for the development of facial bones, hair follicles, and male germ cells in adult mice, and its absence can lead to dwarfism and abnormal follicles.

COVID-19 may harm male fertility and damage the reproductive system.

A gene mutation causes woolly hair in a Syrian patient.

Two siblings were the first reported cases of inheriting both eye coloboma and loose anagen syndrome together.

Woolly hair is a rare genetic condition with no effective treatments.

New mutations in the SLC39A4 gene found in twins help understand the genetic cause of acrodermatitis enteropathica.

A man with Woolly Hair Syndrome had very curly, fragile hair, and doctors used a special scalp examination to diagnose him without invasive tests.

A specific gene mutation causes a severe skin disorder in a family.

CaBP1 and CaBP2 are important for continuous hearing by preventing inactivation of calcium currents in ear cells, with CaBP2 also able to restore hearing when reintroduced.

A boy with Sjogren-Larsson syndrome has skin and muscle symptoms due to a specific enzyme deficiency.

Some people have genetic mutations that make them resistant to vitamin D, leading to rickets even with enough vitamin D intake.

A new severe form of monilethrix syndrome includes hair loss, scalp itching, cataracts, and distinct facial features.

Researchers found a new area on chromosome 2 linked to a genetic hair loss condition.

A Holstein calf in Iran with a severe genetic skin disorder was euthanized due to incurable symptoms.

LIPH mutations in Japan cause varying degrees of hair loss and woolly hair.

A specific gene mutation causes a rare hair loss condition in a Chinese patient.

An Australian with rare hair loss and eye conditions had a gene linked to both, not seen together before.

Over 67 genes linked to ichthyosis help improve diagnosis and treatment.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

The baby’s hair loss was due to a rare genetic condition, not treatable by usual methods.