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The case shows how hard it is to tell apart Multiple Autoimmune Syndrome from other similar autoimmune conditions, but correct diagnosis is key for treatment to work.

The document reports a rare case of ECCL with a new association with optic disc colobomas.

Combining medication and minimally invasive techniques can effectively manage Marine-Lenhart syndrome.

A man developed rare complications after nose surgery, stressing the need for better prevention.

Lichen simplex chronicus on the scalp can be diagnosed by specific hair and skin signs and treated with corticosteroids and therapy.

A woman with chronic hepatitis C had a rare skin condition linked to her illness.

A 61-year-old Filipino man had a skin condition that looked like another disease, making diagnosis difficult.

Woodhouse-Sakati syndrome shows varied symptoms, including hair loss and diabetes, and is common in Qatar due to a specific genetic variant.

A girl initially thought to have a psychiatric disorder was later found to have a lupus-related condition, which improved with proper treatment.

Woodhouse-Sakati syndrome can cause writer's cramp and other varied symptoms, highlighting the importance of genetic testing for diagnosis.

Loose Anagen Syndrome is a hair condition where hairs can be easily pulled out, mainly affecting young girls, and may improve on its own or with treatment.

Netherton's syndrome may have a familial link and doesn't always include atopy.

A man from Brazil had a rare case of leprosy on his scalp, which improved with treatment.

A girl with Becker naevus syndrome has a genetic variant in the ACTB gene related to her symptoms.

A child with a rare scalp condition regrew hair after treatment.

Recognizing minor skin lesions can help identify serious cancer syndromes.

A new genetic mutation in the TRPS1 gene causes Trichorhinophalangeal Syndrome, leading to specific hair, dental, and bone issues.

Early diagnosis and multidisciplinary care, including orthopedic surgery, can prevent long-term disability in IFAP syndrome.

A unique case showed a rare combination of two types of lichen planus on the face.

Mutations in the KLHL24 gene cause a skin disorder in some Russian families.

Catatonia can be a rare sign of lupus, needing careful diagnosis and treatment.

The document describes a woman with familial Parkinson's disease due to a genetic mutation, showing severe symptoms and poor response to treatment, and suggests finasteride may help reduce symptoms in Tourette syndrome.

Two siblings were the first reported cases of inheriting both eye coloboma and loose anagen syndrome together.

Three white adults had a rare scalp condition with increased fat and sometimes hair loss, suggesting it's not limited to black women and might be more widespread.

Early diagnosis and management of Sheehan's syndrome are crucial for improving quality of life and fertility.

A 16-year-old boy with lupus had a rare brain artery issue but fully recovered with treatment.

A 13-year-old boy had both lichen planus and vitiligo, suggesting a possible link between the two conditions.

A 17-year-old girl with Kartagener's syndrome also has unusual skin, hair, and nail issues.

Clouston's syndrome is a rare disorder affecting nails, hair, teeth, and skin, caused by a gene mutation, and currently has no treatment, only supportive care.

Skin lesions in Carney complex are likely caused by a specific group of skin cells that promote pigment production due to a genetic mutation.