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Drumstick leaves extract with amla powder significantly improved anemia in adolescent girls.

TRPS1 is crucial for bone, kidney, and hair follicle development.

Certain gene variants can cause inherited hair diseases, which are important to diagnose and understand for patient care.

Trichorhinophalangeal syndrome causes hair, facial, and bone issues, with no specific treatment beyond gentle care.

Rhodamin B stain is inconsistent for keratin in skin samples.

COVID-19 may be linked to hair loss called Telogen Effluvium, affecting quality of life and self-esteem.

A person with a specific gene mutation had extra teeth, unique jaw and hair features not seen before in this condition.

Dermatologists should consider congenital syndromes like TRPS in young adults with early hair loss.

A family was found with both Trichorhinophalangeal syndrome and Loose Anagen Syndrome, suggesting a genetic connection.

Specific brain and bone imaging findings can help diagnose Trichothiodystrophy.

Trichothiodystrophy causes unusual hair and developmental issues.

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

A new genetic mutation in the TRPS1 gene causes Trichorhinophalangeal Syndrome, leading to specific hair, dental, and bone issues.

A 6-year-old girl with Turner syndrome also had psoriasis, alopecia areata, and trachyonychia.

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

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

A girl with a rare genetic disorder had a unique bone condition, highlighting the need for careful diagnosis and suggesting the disorder might be more common than thought.

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

A rare case of trichothiodystrophy was found with autism, seizures, and mental retardation.

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

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

A child with skin and tooth symptoms was found to have a genetic mutation causing cardiocutaneous syndrome, leading to heart problems.

A girl with Turner syndrome had psoriasis, alopecia areata, and trachyonychia.

Trichoscopy is useful for diagnosing Netherton syndrome in children with skin issues.

Low TRPS1 expression in skin and hair cells is linked to hair problems in Trichorhinophalangeal syndrome.

A man had rare skin tumors with bone formation and cholesterol deposits.

Early diagnosis and a multidisciplinary approach are crucial for children with Trichothiodystrophy and hidden learning disorders.

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

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