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Tjalma Syndrome is a rare condition in people with lupus, causing fluid buildup and high CA-125 levels, but not due to tumors.

Higher disease activity in systemic lupus erythematosus is strongly linked to more internal organ damage.

Some hormone treatments might raise breast cancer risk, while others don't seem to.

Mesenchymal stem cells could help treat aging-related diseases better than current methods.

Two young cats with a severe ear and skin condition improved with immune system-targeting treatments.

Most cases of Temporal Triangular Alopecia are found in early childhood and may be related to genetic conditions.

Trichothiodystrophy is a rare genetic disorder causing hair issues and sometimes linked to DNA repair defects.

A boy with Oculodentodigital syndrome had a unique GJA1 gene mutation causing his symptoms.

Adults with Tatton-Brown-Rahman syndrome may have serious heart problems and need lifelong heart monitoring.

Temporal triangular alopecia is a lifelong condition with hairless patches on the side of the head that may be present from birth.

The document adds two cases of Gomez-Lopez-Hernandez syndrome and suggests including trigeminal anesthesia and scalp alopecia as key diagnostic criteria.

A 3-year-old boy was diagnosed with a rare, non-scarring hair loss condition called temporal triangular alopecia.

Specific brain and bone imaging findings can help diagnose Trichothiodystrophy.

Triangular temporal alopecia can occur in adults and should be correctly identified to prevent misdiagnosis.

Temporal triangular alopecia is a non-scarring hair loss in children, often linked to other health conditions.

Thymoma-associated multiorgan autoimmunity can cause liver damage and affects multiple organs, with limited treatment options and a generally poor prognosis.

Trichoscopy effectively diagnoses temporal triangular alopecia in children.

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

Temporal triangular alopecia is a non-scarring hair loss seen in some Asian children.

Temporal triangular alopecia may be linked to sebaceous nevus and shows a new pinkish background feature.

Two sisters had a rare hair condition without other usual symptoms.

Toe Tourniquet Syndrome is often misdiagnosed.

A woman with a unique syndrome similar to TRPS has a genetic change near the TRPS1 gene, affecting its regulation.

Hair-tourniquet syndrome can cause serious toe injuries in infants but can be treated if found early.

Tiger tail banding and hair abnormalities are reliable indicators for diagnosing trichothiodystrophy.

A new genetic variant causes trichothiodystrophy in two brothers, but their mother may carry it without showing symptoms.

Trichothiodystrophy can be linked to urologic issues and high calcium in urine.

A child was initially wrongly diagnosed with a fungal scalp infection but actually had a non-scarring hair loss condition called Temporal Triangular Alopecia.

The study found that Temporal Triangular Alopecia often starts in early childhood, mainly affects the left side of the scalp, and has no effective treatment except surgery.

A new syndrome, Teelwani Syndrome, combines features of two rare genetic disorders.