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Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

Early and accurate diagnosis is crucial for effectively managing hair loss in lupus and alopecia areata.

A patient with Rothmund-Thomson syndrome showed skin changes, hair loss, and dental defects but no cataracts or skeletal issues.

Most children with CNS tumors on targeted therapy had skin reactions, which were generally treatable without stopping the therapy.

Immune checkpoint inhibitors can increase the risk of autoimmune skin diseases, especially bullous pemphigoid.

Areata-like lupus can mimic alopecia areata but is a form of cutaneous lupus erythematosus.

Patients with cutaneous lupus erythematosus have a higher risk of skin cancer and other cancers.

Mutations in the POC1A gene can cause a unique form of extreme insulin resistance and short stature.

Porphyria cutanea tarda causes skin issues due to an enzyme deficiency.

Chronic kidney disease can cause skin issues that need early recognition and combined treatment for better outcomes.

Managing multiple autoimmune diseases in one patient is very challenging.

Hidradenitis suppurativa may be a type of autoinflammatory skin disease linked to gene mutations and immune system issues.

Most patients with dermatomyositis had skin rash, itching, and muscle weakness, treated mainly with prednisolone and hydroxychloroquine.

Genetic analysis is crucial for diagnosing and managing cerebral arteriopathy.

Ulcerative colitis can cause skin issues due to immune system problems.

Genetic testing confirmed a rare skin disorder in a young girl, which improved with zinc supplementation.

Upadacitinib improved Crohn's disease, atopic dermatitis, and alopecia areata in one patient.

NCSTN gene mutation causes abnormal skin cell differentiation and more inflammation, contributing to Hidradenitis Suppurativa.

A 50-year-old woman with breast cancer developed an autoimmune skin disorder, highlighting the need for thorough checks and team-based treatment.

Neuroendocrine paraneoplastic syndromes often show skin changes, helping early diagnosis and requiring a team approach for best care.

Early detection of Graham-Little-Piccardi-Lasseur syndrome is key for better management.

Netherton syndrome is a genetic skin disorder causing severe skin issues and requires careful treatment to protect the skin barrier.

The patient has Chronic Cutaneous Lupus, a skin condition causing plaques and hair loss.

Recognizing and treating skin symptoms in essential thrombocythemia is crucial for patient quality of life.

A woman with dermatomyositis showed rare skin symptoms, was treated successfully, and her case suggests checking for cancer in similar patients.

Skin symptoms can indicate endocrine disorders and have various treatments.

Patients with mycosis fungoides have a higher risk of heart disease.

Skin symptoms appear in up to 20% of Covid-19 cases.

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

Psychodermatosis is reclassified based on brain-skin interaction, dividing conditions into psychogenic and psychosomatic categories.