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A new severe form of monilethrix syndrome includes hair loss, scalp itching, cataracts, and distinct facial features.

Mogamulizumab can cause hair loss, often linked to a better treatment response.

A patient with Sézary syndrome showed improvement after treatment and the study suggested follicular mucinosis might indicate future lymphoma risk.

Neuromyotonia and morphoea can occur together in the same body areas.

A woman with myotonic dystrophy had multiple skin tumors on her scalp, suggesting a genetic link.

Secondary syphilis in Cali, Colombia, shows high Treponema pallidum presence and challenges in early diagnosis, needing better public health strategies.

A man with severe leprosy developed painless ulcers and numbness, treated successfully with multiple drugs and vitamins.

Benign follicular mucinosis involves immune cells attacking hair follicles.

A woman's skin symptoms led to a diagnosis of systemic AL amyloidosis, but she died from sepsis shortly after.

A 73-year-old woman with Hypopigmented Mycosis Fungoides, a rare skin lymphoma, experienced disease progression despite treatment, emphasizing the need for ongoing monitoring.

A 12-year-old girl was diagnosed with monilethrix, a genetic condition causing fragile, beaded hair that breaks easily, with no effective treatment available.

Moth-eaten alopecia is linked to various skin diseases and requires early treatment to prevent worsening.

The man's rash, hair loss, and vision issues were due to syphilis, not CMV.

Merkel cell polyomavirus can infect and persist in skin cells, evading the immune system, but certain treatments can control it.

Alopecia mucinosa on the face can be linked to mycosis fungoides, a type of lymphoma.

Netherton syndrome causes specific skin and hair changes that help in early diagnosis.

A young cat had a rare fungal infection caused by Microsporum gypseum.

Monilethrix is a genetic disorder causing brittle hair, diagnosed using tricoscopy.

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

Trichodysplasia spinulosa is a rare skin disease in immunocompromised patients caused by a specific virus targeting hair follicle cells.

An 8-year-old girl developed a rare skin condition in a linear pattern on one side of her body after a lung infection, which improved with treatment.

The patient's hair has unique structural differences with alternating bright and dark bands.

A man with a weakened immune system was diagnosed with a rare skin condition called trichodysplasia spinulosa using skin examination techniques.

Folliculotropic mycosis fungoides has unique molecular features and cell interactions that could guide targeted therapy.

The document reports the 19th global case of a rare skin condition in a patient from Colombia.

An 11-month-old boy with Menkes disease had severe brain shrinkage and abnormal blood vessels, and didn't respond well to treatment.

Folliculotropic mycosis fungoides can affect the central nervous system in advanced stages.

A rare scalp infection in a child developed into a kerion with additional skin symptoms.

The woman was diagnosed with systemic lupus erythematosus (SLE) after initial misdiagnosis and improved with proper treatment.