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A woman's pelvic pain and bleeding led to finding and successfully treating a rare benign tumor in her reproductive system.

A woman's excess male hormone symptoms were caused by a rare benign tumor in her ovary.

A deletion in the CDH3 gene causes a rare disorder with short hair and vision loss.

Frontal Fibrosing Alopecia is a hair loss condition mainly affecting postmenopausal women, with unclear causes and various clinical patterns.

Congenital atrichia with papular lesions is often misdiagnosed, and new diagnostic criteria can improve accuracy.

Progeria causes early aging due to a gene mutation, affecting skin, bones, and heart, with treatments aimed at improving life quality.

The document suggests a rare skin condition might be caused by a genetic phenomenon.

The woman's skin and hair symptoms were confirmed as frontal fibrosing alopecia, and while facial papules are common in such cases, there's no effective local treatment, but systemic treatments can help.

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

Hypertrichosis lanuginosa causes excessive fine hair growth, often linked to genetics or cancer, with limited treatment options.

A patient had both chronic cutaneous lupus erythematosus and frontal fibrosing alopecia.

Evaluate prolactin levels with androgen and thyroid tests to rule out endocrine issues in patients with SAHA syndrome symptoms.

A woman's male-like physical changes were caused by two rare ovarian conditions.

A woman with Kallman's syndrome also developed alopecia universalis, a condition not previously linked to Kallman's.

A new genetic mutation was found causing hair and eye issues in a boy.

Harlequin ichthyosis involves abnormal skin cell structures and giant mitochondria, affecting skin and hair.

The report described a unique case of Cronkhite-Canada syndrome with unusual polyps and an association with multiple myeloma.

A rare case of severe scalp hair loss and nail issues in keratosis follicularis was observed.

Black women with CCCA are more likely to have uterine fibroids.

Stopping birth control pills may have triggered a manic episode in a woman with HAIR-AN syndrome.

Becker's Nevus Syndrome is a rare condition with a skin patch and possible bone and muscle abnormalities, treated mainly for appearance.

Basaloid follicular hamartoma's appearance can be similar to other skin conditions, and diagnosis should consider both the look and behavior of the tumor.

Clouston syndrome causes issues with teeth, hair, nails, and skin, and has no cure, but recognition has improved.

Rectangular black granules, solitary yellow dots, and mostly single-hair follicles suggest Loose Anagen Hair Syndrome.

Frontal fibrosing alopecia in families shows similar signs to individual cases and may have a genetic link.

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

Idiopathic hirsutism is the most common cause, followed by PCOS, and insulin resistance should be checked in patients with acanthosis nigricans.

A 20-year-old woman had stable Progressive Hemifacial Atrophy and Vitiligo after treatment, suggesting a possible link between the conditions.

Sorafenib may cause hand-foot and stump syndrome, requiring early detection and management.

New mutations in MBTPS2 reduce its function and cause IFAP syndrome with unusual symptoms.