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Mixed Connective Tissue Disease can develop from overlapping symptoms of several autoimmune diseases, making diagnosis complex.

Cantú syndrome is caused by mutations in the ABCC9 gene.

Woodhouse-Sakati syndrome often causes sexual development issues, hair loss, learning disabilities, deafness, muscle contractions, limb pain, and diabetes.

The patient has a rare skin condition that shows features of two known disorders.

Cantu syndrome, which causes excessive hair growth and skin issues, is due to a mutation in the ABCC9 gene, and understanding this could help develop new treatments for hair diseases.

A teenage girl had both a rare ovarian tumor and a severe form of polycystic ovarian syndrome.

Some medications for inflammation can cause a condition with scalp rashes and hair loss, often linked to Crohn's disease, and may require treatment changes to prevent permanent hair loss.

Hair changes and a high occipital hairline may help diagnose Trichorhinophalangeal Syndrome.

Oral tofacitinib successfully treated a girl's severe skin and hair conditions.

Hypertrichosis involves excessive hair growth and needs careful diagnosis and treatment, considering its psychological effects.

A 21-month-old boy has a rare genetic disorder causing sparse hair due to an LSS gene mutation.

Skin tumor cells in patients with tuberous sclerosis have higher levels of a protein called cathepsin B.

Stopping tight hairstyles can prevent and reduce traction alopecia.

Toxic Shock Syndrome progresses quickly, often involves multiple organs, and is linked to Staphylococcus aureus toxins, with treatment options available but diagnostic challenges remaining.

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

TAF can be identified by excessive skin thickening and clogged hair follicles, helping distinguish it from similar skin conditions.

A trichobezoar caused the girl's recurrent intussusception, and surgery plus psychiatric therapy resolved her symptoms.

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

Proper management of PTSD with psychotherapy and medication can reduce symptoms.

A specific genetic change is linked to mental disorders, intellectual disability, and possibly autoimmune disease in a family.

Thyroid hormone therapy effectively treated the man's rare muscle and heart issues.

A 20-year-old woman was found to have a rare ovarian tumor causing symptoms like acne and a low-pitched voice, which disappeared after the tumor was removed.

Recognize Rapunzel syndrome in children with unexplained stomach issues for timely treatment.

Surgery, especially prostatectomy, effectively reduces detrusor overactivity in bladder outlet obstruction patients.

A patient developed nerve problems as a side effect of a hair loss treatment called tofacitinib.

A young woman developed a bowel obstruction from eating hair from her weave to relieve anxiety.

Consider TFI in facial hypopigmentation diagnoses and confirm with a biopsy.

An 8-year-old girl with vitiligo developed extra hair growth on her knee after using tacrolimus ointment.