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Patchy hair loss from post-herpetic neuralgia can mimic trichotillomania but requires different treatment.

Two boys developed a viral skin infection during chemotherapy, which resolved with improved immune function.

Newborns with ichthyosis need specific care based on their skin type.

The woman has scurvy and needs more vitamin C.

Accurate diagnosis and tailored treatments are crucial for managing hair loss in humans and animals.

External factors like certain shampoos, bacterial infections, and parasites might cause hair defects similar to genetic conditions.

A pet rabbit had a skin infection that was cured with ketoconazole.

A 12-year-old girl was diagnosed with monilethrix, a genetic condition causing fragile, beaded hair that breaks easily, with no effective treatment available.

A rare case of a woman having both lichen planus pigmentosus and classic lichen planopilaris at the same time.

Older adults have a wide range of skin conditions, with dry skin being very common and many also experiencing skin growths, itching, and infections.

Monilethrix is a genetic disorder causing brittle hair, diagnosed using tricoscopy.

A patient grew extra hair on their ears after treatment for testicular cancer, possibly due to hormonal changes or genetics.

Early detection of Lichen Planopilaris is important to prevent worsening and misdiagnosis.

The harlequin ichthyosis mouse mutation causes thick skin and early death, resembling a human skin disorder.

Children with severe ichthyosis and growth failure rarely have nutritional deficiencies or gastrointestinal issues, but may experience chronic dehydration.

Some congenital hair disorders improve in childhood or with treatments like minoxidil and retinoids, while others like Netherton syndrome and trichothiodystrophy have a poor prognosis.

People with plantar corns and calluses may have a higher chance of having metabolic syndrome.

Alopecia can be reversed with timely steroid treatment in VKH and SO diseases.

A man had a unique case of three skin conditions happening together.

A woman with a new PTCH gene mutation has both Gorlin syndrome and severe hair loss.

The document explains how to identify different hair problems using a microscope.

Syphilitic alopecia can look like alopecia areata, so careful diagnosis is important.

A 19-month-old boy with a rare hair disorder showed mild improvement with treatment, but his family chose gentle hair care due to limited success.

Older men's scalp damage increases with age and sun exposure, a baby girl in the Philippines has Schimmelpenning syndrome, and thyroid screening is advised for children with hair loss and certain risk factors.

The document reports a unique case of woolly hair with a combination of conditions not previously seen together.

Tay syndrome is a unique genetic disorder causing skin, hair, and developmental issues.

The document concludes that an inherited nail condition often improves on its own, and spironolactone effectively treats acne in women.

A child with skin and tooth symptoms was found to have a genetic mutation causing cardiocutaneous syndrome, leading to heart problems.

Chronic Acrodermatitis Enteropathica can persist into adulthood and requires careful zinc treatment.