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Clouston syndrome can lead to skin cancer, so monitoring is crucial.

Hypertrichosis causes excessive hair growth and needs psychological support due to its impact on self-esteem.

A woman with X-linked chronic granulomatous disease developed lupus-like skin lesions, improved with treatment, suggesting a unique skin condition in carriers.

Hair-shaft abnormalities can indicate neurological disorders, some of which are treatable.

Imatinib can cause hair loss due to lichen planopilaris.

A rare case links early-onset alopecia universalis and nephrotic syndrome, suggesting genetic immune issues.

A child with trichothiodystrophy also had autoimmune thyroiditis and anemia, which is a new finding.

A new mutation in the STING protein causes a disease with lupus-like symptoms and responds well to a specific inhibitor treatment.

Mitochondrial dysfunction and oxidative stress may play a role in Lichen Planopilaris.

A six-year-old boy with excessive hair growth and other symptoms may have a genetic link on chromosome 17q, requiring regular medical follow-ups.

Pseudopelade of Brocq is a unique hair loss condition, but its cause and development are still not fully understood.

A girl with a rare genetic disorder had a unique bone condition, highlighting the need for careful diagnosis and suggesting the disorder might be more common than thought.

Gender-specific analysis could improve treatment for childhood systemic lupus erythematosus.

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

Dermoscopy is useful for diagnosing lichen planopilaris and certain features may relate to disease duration, age, and gender.

Early diagnosis using eye tests and lab markers can improve treatment for pediatric Sjögren's syndrome.

Graves' disease mainly causes hyperthyroidism in children, especially girls aged 10-14, with treatment options including medication, radioactive iodine, and surgery.

A rare skin condition in a 17-year-old was diagnosed late, stressing the need for careful evaluation and genetic testing.

Lichen planus pigmentosus causes dark skin patches and is treated by avoiding triggers and using anti-inflammatory medications.

Siblings with signs of virilization should be tested for non-classical congenital adrenal hyperplasia, which does not affect adult height but may impact fertility and well-being if untreated.

Low-dose Ritlecitinib may help children with stubborn Alopecia Areata.

Uncombable hair syndrome causes dry, frizzy hair that can't be combed flat, seen in a young child.

Clim proteins are essential for maintaining healthy corneas and hair follicles.

Facial lichen planopilaris may be triggered by shaving and mustard oil, and early detection is crucial for better treatment outcomes.

An infant with complete hair loss was diagnosed with a genetic disorder affecting hair growth.

VHL disease can cause early paragangliomas, needing lifelong monitoring.

Skin lesions in Carney Complex are caused by a gene change in some skin cells that leads to increased pigmentation and may lead to tumors.

Seven patients were misdiagnosed with discoid lupus instead of lichen planopilaris due to similar symptoms, showing the need for careful diagnosis in scarring hair loss conditions.

A gene deletion in mice causes weak protein, immune issues, hair loss, airway problems, and wasting disease.