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TTD hair is brittle due to fewer sulfur amino acids and unstable disulfide bonds.

Triangular temporal alopecia is a benign hair loss pattern best diagnosed with dermoscopy, with limited treatment options like surgery and hair transplantation.

Buschke-Ollendorff syndrome is a rare genetic disorder causing skin and bone changes, with some cases also showing ADHD or developmental delays.

A boy with early puberty and laughing seizures was treated, stopping seizures and slowing puberty.

Accurate diagnosis is crucial to distinguish between PCOS and rare ovarian tumors in teens with similar symptoms.

Shaving and avoiding brushing improved the patient's beard hair condition.

Trichoscopy helps accurately diagnose Netherton syndrome, often mistaken for atopic dermatitis.

Trichothiodystrophy causes abnormal protein deposits and distortion in hair follicles.

Prompt diagnosis and treatment of hair tourniquet syndrome involving the uvula are crucial to prevent severe complications.

A patient with Myotonic dystrophy type 1 had multiple tongue hemangiomas and was sensitive to anesthesia.

Tofacitinib effectively treated a woman's complex autoimmune and autoinflammatory disorders.

Satoyoshi syndrome is likely an autoimmune disease.

An infant developed excessive hair growth after a bone marrow transplant and cyclosporine treatment.

A new TP63 mutation was found in a baby with EEC syndrome, showing the need for TREC testing to check for immune issues.

Tattoos may trigger autoimmune symptoms in some people.

A girl initially thought to have a psychiatric disorder was later found to have a lupus-related condition, which improved with proper treatment.

An 8-year-old boy with neurofibromatosis type one also has rare hair and eye disorders.

Tofacitinib helped an 8-year-old child recover from a type of hair loss that is hard to treat.

Clinicians should be aware of alternating thyroid conditions and their treatment.

Two specific SNPs in the TRPS1 gene cause excessive hair growth by altering the protein's structure.

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

A girl with Pitt-Hopkins syndrome developed curly hair as a rare side effect from the epilepsy drug perampanel.

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

Early recognition and treatment of VATS in transplant patients improve outcomes.

Hypothyroidism may cause vertigo symptoms like BPPV.

Early recognition and multidisciplinary management of Whitaker syndrome can improve patient outcomes.

Trichorrhexis nodosa is mainly caused by hair trauma and improves with gentler hair care.

Prenatal diagnosis of trichothiodystrophy is possible in the second trimester using fetal eyebrow biopsy, with sulfur content analysis being more reliable.