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Many children with alopecia areata also have other autoimmune diseases.

Managing multiple autoimmune diseases in one patient is very challenging.

The document concludes that a thorough history, physical exam, and specific tests are crucial for diagnosing and managing hair loss effectively.

Most vitiligo patients in Makkah are young women, often with family history and thyroid issues.

Relapsing hepatitis A can cause prolonged abnormal liver tests even without symptoms.

A multidisciplinary approach is crucial for treating complex cases of Rapunzel syndrome in children.

Diphencyprone therapy can effectively treat severe hair loss in motivated patients.

Alopecia areata was most common in people in their 30s and 40s, with some family history and a higher relapse rate, and larger bald areas responded better to specific immunotherapy.

Accidentally eating a topical steroid may rarely cause acute generalized pustular psoriasis.

Myo-inositol supplements may improve insulin sensitivity and help with conditions like PCOS and gestational diabetes, but more research is needed.

Pediatric androgenetic alopecia is linked to obesity, family history, hormonal imbalances, and requires personalized treatment including managing comorbidities.

Minoxidil improved hair growth in a child with a rare genetic disorder.

A 23-year-old Syrian woman has two rare hair disorders, and avoiding hair treatments plus using vitamins and minoxidil may help.

A rare skin disorder, Ichthyosis with confetti, has no cure but treatment focuses on managing symptoms with moisturizers.

PCOS and related metabolic issues often run in families.

Doctors should consider SLE in males even if antinuclear antibody tests are negative.

Minoxidil effectively improved hair loss in a teenage girl with androgenetic alopecia.

People in Jeddah know about Vitamin D and its sources but are unclear on how much they need daily, and while many women take supplements, attitudes towards increasing Vitamin D levels vary.

A man developed male breast cancer after four years of finasteride treatment for an enlarged prostate.

In the Jazan region of Saudi Arabia, hair loss is common, especially among women, older people, and those with higher education and BMI. Stress, poor nutrition, and hormonal changes are key causes, but many don't seek medical help.

Women with PCOS are at high risk of glucose metabolism issues and heart diseases, especially if overweight, highlighting the need for early intervention.

Three siblings with a genetic form of rickets showed different symptoms of the disease.

Genetic testing for cancer risk can lead to early and life-saving treatments in people without symptoms.

High androgen levels in Chinese women with PCOS are linked to a higher risk of diabetes and obesity.

Minoxidil users may experience hair discoloration, especially with long-term use and a family history of gray hair.

Genetic variants linked to ten skin diseases were found, showing both immune and non-immune factors play a role.

Kennedy's disease leads to muscle weakness and sensory issues, has no cure but manageable symptoms, and future treatments look promising.

The patient likely has Chrousos syndrome, a rare condition causing insensitivity to glucocorticoids, requiring high-dose dexamethasone treatment.

A specific thyroid hormone resistance mutation may be linked to different types of hair loss.

25% of women in North Sudan have traction alopecia, linked to family history and hair treatments, highlighting the need for better hair care awareness.