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A cystic fibrosis patient developed Cushing's syndrome from a drug interaction between itraconazole and budesonide, which improved after stopping the medications.

Hair or fiber wrapped tightly around a toe can lead to serious injury if not treated quickly.

The clinical signs of Adams-Oliver syndrome can vary greatly, even among family members.

Mercury allergy linked to specific genes may contribute to burning mouth syndrome, and silicon might play a role in maintaining healthy hair.

Taking L-tryptophan supplements might cause a condition similar to scleroderma in some people, which can get better after stopping the supplement and starting corticosteroid therapy.

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

Gene sequencing is essential for diagnosing junctional epidermolysis bullosa.

A 4-year-old girl had a rare hair disorder affecting only part of her scalp.

Poliosis circumscripta is a patch of white hair caused by lack of melanin, linked to genetic and acquired conditions.

Screen young women with menstrual issues, acne, or excess hair for high cortisol to avoid misdiagnosis.

A young woman with skin issues and weight loss improved after treating her pancreatitis and using skin treatments.

A woman had a unique skin growth with hair follicle, oil glands, fat cells, spindle cells, and nerve fibers.

Women with nonclassic congenital adrenal hyperplasia experience more sexual dysfunction and distress.

A boy with chromosome 13q deletion syndrome developed eye cancer, a woman with breast cancer lost vision due to a rare side-effect of her treatment, a man's vision worsened after using a hair loss drug, and two rare disorders were discussed. Optical Coherence Tomography is useful for diagnosing and monitoring these conditions.

All parts of the CLASI-A score are important for assessing skin activity in cutaneous lupus erythematosus.

Vogt-Koyanagi syndrome often leads to partial or complete blindness and responds poorly to treatment.

A teenage girl had both a rare ovarian tumor and a severe form of polycystic ovarian syndrome.

Doctors often miss Hair Tourniquet Syndrome, which can lead to serious damage if not treated quickly.

A Jordanian family with Clouston syndrome has a common GJB6 gene mutation.

The patient with both scarring and non-scarring hair loss showed complex immune reactions and improved with steroid treatment.

The man had myotonia, which caused delayed hand grip relaxation.

Cystic panfolliculoma is a rare, harmless tumor that can be confused with other skin tumors.

The document suggests a rare skin condition might be caused by a genetic phenomenon.

One twin girl has Loose anagen syndrome with poorly anchored hair, diagnosed with a simple hair pull test, while her identical twin does not have the condition.

Rapunzel syndrome can show vague symptoms and needs long-term psychiatric care to prevent recurrence.

Ceramide Synthase 4 is crucial for healthy skin barrier function.

A new genetic mutation in the CDH3 gene causes hair loss and eye problems in young people.

Hair-thread Tourniquet Syndrome, where hair or thread tightly wraps around a body part, is not rare and requires early detection to prevent serious damage.

A rare skin condition usually found near the eyes was found on a farmer's scalp.

Recognizing CVG can help diagnose systemic amyloidosis early.