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A patient with "strawberry gingivitis" improved after correct treatment for Granulomatosis with polyangiitis, highlighting the need for early diagnosis.

Azathioprine can help with relapses and disability in NMOSD but has more side effects and needs more research.

The woman was diagnosed with lichen sclerosus, a rare skin condition, after initial misdiagnosis and ineffective treatments.

The study suggests that motor neurons created from stem cells of patients with spinal and bulbar muscular atrophy show signs of the disease, including changes in protein levels and cell functions.

Azathioprine can cause hair loss and matted hair.

A child with skin and heart issues had rare genetic mutations affecting skin and heart cell cohesion.

Long COVID affects over half of COVID-19 survivors, causing a range of symptoms like fatigue and neurological issues, with no specific treatment yet.

Young adults have about 230,000 tactile nerve fibers, decreasing 5-8% per decade with age.

Genetic variants can affect valproic acid's effectiveness, side effects, and levels in epilepsy treatment.

A woman's chronic head pain after hair transplant surgery was cured by removing a post-traumatic neuroma.

Sensory neuron and Merkel cell changes in the skin happen independently during normal skin maintenance.

Early diagnosis and treatment of TPP can prevent complications.

A 7-year-old dog with a rare autoimmune disease was euthanized due to severe anemia and poor prognosis.

Nail abnormalities in children can indicate deeper health issues.

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

A man with Cronkhite-Canada syndrome had all 20 nails detach but improved with treatment.

ANE syndrome is caused by a mutation in the RBM28 protein that disrupts ribosome assembly.

Nagashima-type palmoplantar keratosis in Asians is caused by a SERPINB7 gene mutation.

Monilethrix severity varies and may be influenced by other genetic or environmental factors.

A cat with a rare pancreatic tumor and diabetes died despite treatment, showing similar symptoms to a human condition.

SLE and DM can coexist but are rare and need careful evaluation.

EPDS and MS might share an immune-related cause.

Epidermal neural crest stem cells from hair follicles can help repair nerve injuries.

Trichodynia is a challenging scalp condition to treat, needing gentle care and more research for better solutions.

Zouboulis syndrome is a rare condition that helps diagnose monosomy 18p early.

BMP4-related anomalies can cause a wide range of eye, brain, and hand/foot problems, and new cases show this variability.

The brothers have congenital ichthyosis, and the older brother's eye issues are due to different genetic mutations.