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

Graham-Little syndrome causes scarring hair loss and skin bumps.

A Chinese man with KID syndrome had a new mutation in the GJB2 gene.

Early and accurate diagnosis of congenital smooth muscle hamartomas is crucial to distinguish them from other conditions.

A specific gene mutation causes hair loss and potential eye issues, even if vision seems normal.

A 20-year-old woman with a rare form of Turner syndrome showed improvement with hormonal therapy and needs comprehensive care.

AMN can cause bladder problems due to nerve damage.

Netherton's syndrome may have a familial link and doesn't always include atopy.

A six-year-old boy with excessive hair growth and other symptoms may have a genetic link on chromosome 17q, requiring regular medical follow-ups.

Trichothiodystrophy is a condition with brittle hair and various physical and mental issues due to low sulfur in proteins.

Biotinidase deficiency has various symptoms and can be treated with biotin supplements.

Congenital Triangular Alopecia is a rare, non-scarring hair loss that can be surgically treated in females for cosmetic reasons.

Patients with hair loss are much more likely to have body dysmorphic disorder than general dermatology patients.

A Chinese male with a new genetic mutation has a skin condition and severe urinary issues, with treatments having mixed success.

Pseudopelade can affect both the scalp and beard, causing hair loss.

A rare genetic disorder causes sparse hair and vision loss due to a CDH3 gene mutation.

A new MTX2 gene mutation caused a severe genetic disorder in a young Chinese girl.

Rapid virilization should be checked for possible ovarian or adrenal cancer.

Nevoid basal cell carcinomas start in the skin and hair follicles.

Permanent hair loss after bone marrow transplant can be caused by chemotherapy or chronic graft-versus-host disease.

A rare case of severe scalp hair loss and nail issues in keratosis follicularis was observed.

A rare autoimmune condition, Satoyoshi syndrome, can start in adults and improve with immunosuppressive treatment.

Folliculin deficiency causes problems with cell division and positioning due to disrupted RhoA signaling and interaction with p0071.

A pregnant woman with Cushing Syndrome got worse and sadly passed away.

Cystic panfolliculoma is a rare, harmless tumor that can be confused with other skin tumors.

A rare case linked complete hair loss to both pancreas and gallbladder cancer.

Consider Sertoli-Leydig cell tumors in Peutz-Jeghers syndrome patients with adnexal masses.

Cronkhite-Canada syndrome can be diagnosed without gastrointestinal polyps if there is severe mucosal atrophy and edema.

A woman with both Cronkhite-Canada syndrome and myelodysplastic syndrome improved significantly with corticosteroid treatment.

A genetic duplication on chromosome 5 was linked to a woman's unique combination of medical conditions.