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A 36-year-old man had unusual skin lesions on his face without hair loss.

The document concludes that careful diagnosis is crucial for chromosome 13q deletion syndrome, tamoxifen can cause reversible eye damage, finasteride may be linked to cataracts, and OCT is useful for diagnosing macular diseases.

IVIG therapy significantly improved symptoms in a patient with APS-2 and SPS.

A man with a rare skin condition and a new gene mutation developed high calcium levels due to his treatment.

Women with lichen planopilaris often have thyroid disease, depression, anxiety, and may respond to treatment with slowed disease progression.

The 736T>A mutation in the LIPH gene is common in Japanese people with autosomal recessive woolly hair.

Early recognition of skin lesions in Birt-Hogg-Dubé syndrome is crucial for detecting renal tumors early.

A 2-year-old boy was diagnosed with a rare genetic condition causing fragile hair, intellectual issues, and short stature.

Dermoscopy is useful for diagnosing lichen planopilaris and certain features may relate to disease duration, age, and gender.

A 13-year-old boy with a rare genetic condition survived a heart attack and improved with treatment.

Metreleptin treatment significantly improved metabolic health in a boy with congenital generalized lipodystrophy.

A 14-year-old girl with no menstrual period was diagnosed with Swyer Syndrome and treated for a related cancer risk.

Certain SPINK5 gene mutations are common in Israeli families with Comèl-Netherton syndrome.

Hyperaesthetic leucotrichia in horses causes painful, recurring skin lesions and hair color changes, especially in Arabian and American paint horses.

SCAD can indicate ANA-negative lupus, especially in women with unusual symptoms.

Careful histologic examination is crucial to differentiate types of bullous lesions in cutaneous lupus erythematosus.

The lump on a woman's scalp was a rare, potentially cancerous tumor from the hair follicle, not a common cyst.

A rare case showed alopecia areata and lichen planus occurring together in one person.

Dissecting cellulitis may have genetic links and can cause permanent hair loss.

Rhupus is a complex syndrome that combines rheumatoid arthritis and lupus, making diagnosis challenging.

A 29-year-old woman with symptoms of both lupus and rheumatoid arthritis improved with specific medications.

Lichen planopilaris may be an autoimmune disease causing hair loss due to immune system issues in hair follicles.

Lichen planopilaris patients are more likely to have hypothyroidism.

A new mutation caused a rare hair disorder in a Polish girl, not inherited from her family.

Ixekizumab may be an effective first treatment for a rare skin condition causing hair loss.

Early identification of lupus through skin signs and blood tests is crucial in India.

A 14-year-old girl with a condition that makes her hair easy to pull out also has a hair-pulling disorder, and treatment helped but she relapsed after a year.

Early diagnosis and treatment of Lichen Planopilaris are crucial to prevent permanent hair loss.

The study found that males with KFSD had severe skin and eye symptoms, while female carriers had milder symptoms.

A 15-year-old boy's skin and hair condition worsened due to improper treatment, leading to severe health issues.