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Intravenous calcium therapy is a safe and effective treatment for a rare type of rickets.

Acitretin improved monilethrix symptoms temporarily, but they returned after stopping treatment.

A baby boy's toe was saved from damage caused by hair strangulation by quick surgical treatment.

PNH can occur in patients with SLE, so doctors should be aware of this.

Woodhouse-Sakati Syndrome can include unique symptoms like liver issues and low growth hormone.

Temporal triangular alopecia in infants is mostly seen in males at birth, with unique features that help with diagnosis.

Polyomavirus A2 infection in newborn mice caused hair follicle tumors.

The Lanceolate hair-J mutation in mice mimics human hair disorders like Netherton's syndrome.

Two brothers from Bangladesh were diagnosed with X-linked adrenoleukodystrophy, showing neurological and adrenal symptoms.

Consider systemic lupus erythematosus in patients with unexplained intracranial hypertension.

Syphilis can mimic other diseases, making diagnosis challenging, but proper testing and treatment are effective.

A rare skin condition caused scarring hair loss on the scalp.

A young woman with lupus developed tuberculosis due to weakened immunity from her medication, showing the need for better TB screening in such patients.

Topical immunotherapy for alopecia areata may work by creating immune cell clusters in the skin.

Hantavirus survivors often face long-term health issues, needing ongoing care.

Some people with schwannomatosis have a new type of mutation in the LZTR1 gene.

The mouse model showed defects in adult stem cell maintenance related to Hutchinson-Gilford progeria syndrome.

Alopecia areata can be an early sign of Hodgkin’s lymphoma and may improve with lymphoma treatment.

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

A 23-year-old man has a benign, non-progressive hair loss patch that doesn't respond to treatment but can be cosmetically treated.

Trichorrhexis invaginata can occur with tinea capitis, though it's rare.

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

People with myotonic dystrophy type 1 tend to develop basal cell carcinoma at a younger age but not more frequently than others.

Specific keratin gene mutations can cause monilethrix.

Mutations in the hairless gene cause a rare form of permanent hair loss.

Autoimmune hair loss may be linked to increased Th1 and Th17 cells and decreased Th2 cells.

Trichodysplasia spinulosa can occur after a heart transplant due to immunosuppressive drugs.

Herpes simplex virus infections should be considered in pemphigus patients to avoid unnecessary changes in treatment.

A brain injury can lead to compulsive hair-pulling and psychosis-like symptoms, needing comprehensive treatment.

Alopecia universalis from alemtuzumab in multiple sclerosis can be reversed with specific treatments.