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Necrobiosis lipoidica may need new criteria for accurate diagnosis due to similarities with another condition.

A rare skin disorder, nevus comedonicus, can appear on one side of the body following Blaschko's lines.

The man has a genetic skin condition called pachyonychia congenita.

The same genetic mutation in Sjögren-Larsson syndrome can lead to different levels of severity, suggesting other factors influence the symptoms.

An isolated episcleral plasmacytoma can mimic episcleritis, making diagnosis challenging.

The study suggests that acne keloidalis nuchae is linked to conditions like pseudofolliculitis barbae, scalp infections, metabolic syndrome, and is more common in males with an average onset age of 25.4 years.

The study found increased skin pigmentation and variable melanocyte density in a patient with Addison's disease.

Anti-MND antibodies are present in various diseases, not just PBC, and their levels don't correlate with disease activity or skin symptoms.

AKN is a chronic scalp condition in African-descended males, treated with topicals, antibiotics, steroids, and sometimes surgery or laser.

RET mutation is important in familial medullary thyroid carcinoma, and BRAF mutation in papillary thyroid carcinoma is linked to more aggressive cancer and higher death rates.

Some patients with a type of skin lymphoma can experience a rare, non-scarring hair loss that looks like another hair loss condition but has distinct features.

Taiwan reported its first case of a rare scalp condition with no clear cause or treatment.

Recognizing the link between certain autoimmune disorders and neurological conditions can improve diagnosis and treatment.

A new genetic mutation in the TRPV3 gene causes Olmsted-like syndrome in a Mongolian family.

Recognizing specific scalp patterns can help diagnose hair loss linked to breast cancer spread.

If someone has scaly skin, muscle stiffness, and intellectual disability, doctors should consider Sjogren-Larsson Syndrome, but other conditions if more symptoms are present.

The patient's symptoms improved with treatment but recurred when the steroid dose was reduced, requiring ongoing therapy.

Punctate follicular porokeratosis is a skin condition with specific features seen in hair follicles.

An 18-year-old boy had a harmless skin nodule near his nose with hair and oil glands inside.

A 62-year-old woman got a lump on her eyelid from tiny mites, which is the first time this has happened.

Mice with the 'lanceolate hair' mutation have abnormal hair and skin similar to human Netherton's syndrome.

Epidermal nevi are skin cell clusters linked to various syndromes.

A 46-year-old man showed symptoms of a rare condition usually seen in postmenopausal women, highlighting the need for dentist-dermatologist collaboration.

A rare ovarian tumor was diagnosed in a woman from North Brazil, and surgery is the preferred treatment.

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.

Trichoscopy can reveal specific hair and scalp changes in linear morphea.

Seborrheic keratosis is a common, harmless skin growth that can look like cancer, so it may need a biopsy.

Treatment improved some symptoms but not all.

A woman with lymphoma had a rare skin rash on her scalp and forehead, which was hard to diagnose but responded well to treatment.

A rare form of lupus caused hair loss and skin bumps, diagnosed through biopsy, improved partially with treatment.