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Early referral to a pediatric rheumatologist and thorough evaluation are crucial for treating complex overlap syndromes effectively.

Children with alopecia areata, especially with Down syndrome or thyroid issues, should be screened for thyroid disease.

The patient had a severe itchy rash and hair loss in the armpits.

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

Monilethrix is a genetic hair disorder causing fragile, beaded hair with no effective treatment.

A woman with myotonic dystrophy had multiple skin tumors on her scalp, suggesting a genetic link.

A postmenopausal woman had rare symptoms due to a possible ovarian tumor, needing thorough evaluation.

The report concludes that atypical Brauer nevus is more common in males, present at birth, and often misdiagnosed due to its unusual scalp locations.

Diagnosing and treating monilethrix is challenging when it occurs with other hair disorders.

A 73-year-old woman's unusual hair loss and growth led to the discovery of a rare condition causing too much testosterone, which improved after her ovaries were removed.

Tattoos may trigger autoimmune symptoms in some people.

A neck lesion misdiagnosed as benign was later treated successfully with Mohs Micrographic Surgery.

A woman's severe skin reaction was caused by an allergy to a skin treatment.

Recognizing eyebrow hair loss linked to a rare skin condition is crucial for proper treatment.

Myotonic dystrophy should be considered in patients with hair thinning, and genetic counseling is important.

Some cases of folliculotropic mycosis fungoides may progress slowly and not need aggressive treatment.

A woman with a rare autoimmune disorder had a blister on her eye and unique immune reaction, which was effectively treated with medication.

Congenital triangular alopecia is more common than thought and some treatments can be beneficial for appearance concerns.

Removing both ovaries may better treat increased male hormone levels and related symptoms in postmenopausal women when hormone therapy doesn't work.

A woman with a rare ovarian tumor and hyperparathyroidism improved after surgery, highlighting the need for reporting unusual cases to understand and manage rare diseases.

The study concludes that a genetic mutation in TFM mice leads to reduced androgen receptor activity, affecting the body's response to male hormones.

A man with a skin nodule was diagnosed with a rare skin condition called cutaneous focal mucinosis, which can be confused with other skin cancers.

TB lymphadenitis can occur in people with weakened immune systems, like those with SLE.

Identical twins with a rare KRT 86 gene mutation both have the hair disorder monilethrix.

A rare skin condition in a boy is likely due to a specific genetic mutation pattern.

Hair-shaft abnormalities can indicate neurological disorders, some of which are treatable.

A 16-year-old girl with a hair-eating disorder needed surgery to remove a hairball from her stomach and small bowel.

A mutation in the EDNRA gene causes Oro-Oto-Cardiac syndrome, affecting face and heart development.

Sweat duct differentiation in trichilemmal cysts is very rare and can be successfully removed with surgery.

Psoriasis can cause rare vulval scarring.