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A woman with lymphoma had a rare skin rash on her scalp and forehead, which was hard to diagnose but responded well to treatment.

About 15% of adolescent girls in a region of India have Polycystic Ovarian Syndrome, which is more common in those born by cesarean, with wisdom teeth, or with central obesity.

Cronkhite-Canada syndrome may be more treatable and less severe than previously thought.

Early diagnosis and nutritional support are crucial for managing Cronkhite-Canada Syndrome.

Routine genetic testing is crucial for early diagnosis and better management of Turner’s syndrome with 21-hydroxylase deficiency.

Narrowband UVB therapy significantly improved a child's rare skin condition.

Strontium ranelate helps cartilage growth by blocking a specific cell pathway.

Early diagnosis and treatment with corticosteroids can improve outcomes in Cronkhite–Canada syndrome.

An 8-year-old boy recovered from a rare case of penile tourniquet syndrome after hair removal surgery.

Early dermatological referrals are important for women and girls with Turner syndrome to improve life quality.

Cortisone reductase deficiency can cause high androgen and cortisol levels and may be missed in women with similar symptoms.

Two sisters with Netherton's syndrome had skin and hair issues, needing special diet and ointments.

Early diagnosis of PSIS can lead to normal height with growth hormone and testosterone treatment.

Cantú syndrome may be linked to pituitary adenomas.

Two boys had a rare skin condition needing to be differentiated from similar disorders, with unclear inheritance due to few cases.

A 17-year-old with Netherton syndrome has dry, itchy skin, brittle hair, and high IgE levels, treated with antihistamines and emollients.

Specific brain and bone imaging findings can help diagnose Trichothiodystrophy.

Topical minoxidil may help treat a rare genetic hair condition with no fully effective treatments yet.

A new genetic change in the DSC3 gene is linked to a rare condition causing hair loss and skin blisters in a child.

Graham-Little syndrome causes hair loss and skin bumps, with difficult treatment options.

Patients with both connective tissue disease and acid reflux are more likely to have certain symptoms and physical signs.

Triptorelin helps evaluate hormone production in Sertoli-Leydig cell tumors.

Dr. Conroy's book on Morgellon's disease lacks credible evidence and scientific validity.

PCOS is a common hormonal disorder in women, marked by symptoms like hair growth and menstrual issues, and requires personalized treatment.

The most common PCOS type in adolescents is hyperandrogenic with polycystic ovaries.

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

Oral steroids may effectively treat recurrent intussusception in children with ILH, possibly avoiding surgery.

A chromosomal change may cause ectodermal dysplasia and developmental issues in a child.

A potential genetic link between Werner syndrome and kidney disease was suggested.

A rare hair regrowth pattern can occur in some people with alopecia areata.