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Tjalma Syndrome is a rare condition in people with lupus, causing fluid buildup and high CA-125 levels, but not due to tumors.

Intralesional steroid injections can effectively treat calcinosis and ulcers in scleroderma.

Oral calcitriol helped improve scleroderma and hair regrowth in a young woman.

Steroid sulfatase in hair follicles may be a target for treating hair loss.

Early diagnosis and genetic counseling are crucial for managing adrenoleukodystrophy.

A man's rare tumor caused unusual nerve-related symptoms that improved after surgery.

Early biopsy is crucial for diagnosing rare skin sarcoidosis, improving treatment.

A sugar glider had a rare skin cancer that worsened despite treatment, highlighting the need for thorough checks in exotic pets.

VHL disease can cause early paragangliomas, needing lifelong monitoring.

A potential link exists between unexplained hormone deficiency, hair loss, and testicular tumors, suggesting thorough screening is needed.

Deleting Smad4 and PTEN genes in mice causes rapid, invasive stomach cancer.

Steroid use can cause a rare eye condition called central serous retinopathy, which can lead to permanent vision damage.

The L457(3.43)R mutation in the human lutropin receptor causes increased activity and hormone insensitivity, leading to precocious puberty.

Testosterone increases seizure risk through its conversion to specific neurosteroids.

Using GnRHa agonists helps diagnose and treat ovarian hyperthecosis when surgery isn't possible.

Some aggressive scalp cancers are hard to treat and can be deadly, even when removed with specialized surgery.

A novel CLDN1 mutation in a 2-month-old with NISCH showed improvement with symptom management.

Krt15+ cells in mice can resist radiation, regenerate tissue, and start tumors, suggesting new cancer treatment targets.

PCFCL may have unrecognized subtypes and needs more research.

The Trichodysplasia spinulosa virus protein can cause abnormal hair growth in mice.

The cause and importance of misplaced oil glands in the hair follicle are not well understood.

A 20-year-old woman with a rare form of Turner syndrome showed improvement with hormonal therapy and needs comprehensive care.

Ripretinib is effective and safe for treating advanced GIST in Chinese patients, particularly for non-gastric GISTs.

Stem cell behavior varies with stimuli, and lineage changes can happen without affecting stem cell division.

A 21-year-old had a rare developmental anomaly with a misplaced sebaceous gland in a hair follicle.

Trichilemmal carcinoma is a rare skin cancer that requires careful diagnosis and follow-up.

A new DSG4 gene mutation causes hair defects in a young girl.

Some skin tumors from hair follicles and glands can be linked to genetic syndromes and may be benign or malignant.

Personalized treatment based on detailed tumor analysis successfully managed and reduced the patient's aggressive hair follicle cancer.

A 21-month-old boy has a rare genetic disorder causing sparse hair due to an LSS gene mutation.