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MILL molecules are unique immune proteins in mice that don't need TAP to appear on cell surfaces.

A 15-year-old boy was correctly diagnosed with a rare skin condition after initially being misdiagnosed.

Monilethrix, a genetic hair disorder causing fragile hair, affects three generations in a family.

The Persian cat has a skin infection caused by a fungus, treatable with antifungal medication.

The p.P25L mutation in the KRT5 gene causes a rare skin condition that worsens over time and may lead to hair loss starting in young adulthood.

Histopathology is crucial for accurately diagnosing and predicting outcomes of skin adnexal tumors.

Psychosis can be an early sign of neuropsychiatric lupus, treatable with tailored medication.

A 93-year-old woman developed a rare scalp condition after therapy, which improved with steroids, not antibiotics.

Monilethrix has no effective treatment, but avoiding hair trauma helps manage it.

Discoid lupus erythematosus can be mistaken for a skin infection, complicating diagnosis and treatment.

A girl with lupus had unusually long and thick eyelashes, a rare symptom of her condition.

A new medical syndrome may include skin changes, hair loss, sweating issues, bone malformations, leg swelling, and low cortisol.

A young man had a rare skin condition causing hair loss and forehead lesions.

Adjusting the medication tacrolimus resolved a boy's red nail beds after a stem cell transplant.

The document concludes that specific hair and blood vessel abnormalities in infants with seizures and developmental issues may indicate Menkes disease, which lacks a cure and is often fatal by age 3.

Lichen planus may be associated with a higher risk of metabolic syndrome.

Hair follicle and adipose cell vesicles both protect neurons and reduce inflammation similarly.

Neuroendocrine paraneoplastic syndromes often show skin changes, helping early diagnosis and requiring a team approach for best care.

Children with alopecia areata, especially with Down syndrome or thyroid issues, should be screened for thyroid disease.

Frontal fibrosing alopecia can occur in children, not just postmenopausal women.

The document found differences in lesion distribution and microscopic features among trichostasis spinulosa and similar skin conditions.

Onycholemmal horn is a rare nail tumor in elderly women, treated by surgical removal.

PRP injection for hair growth can cause reversible vision loss due to inflammatory optic neuropathy.

Early diagnosis of Bloch-Sulzberger Syndrome is crucial to prevent severe complications.

Eyelash loss can be a sign of thyroid problems.

A woman's increased facial hair and hair loss were caused by a rare ovarian tumor, cured by surgery.

UVA1-light therapy successfully treated a child's skin condition, mycosis fungoides.

Lower lipin 1β in belly fat is linked to insulin resistance in people with polycystic ovary syndrome.

Early recognition and evaluation of nevus sebaceus are crucial to detect and manage potential cancerous changes.

Some skin growths with mucin can form hair follicles and resemble skin cancer, but a special stain can help tell them apart.