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Chronic lupus and frontal fibrosing alopecia can occur together, but their connection is unclear.

A mother and daughter with similar hair loss conditions and identical HLA types suggest a genetic link between the conditions.

IPL treatment can significantly reduce hair in faun tail but may need local anesthesia.

Woman has discoid lupus, frontal fibrosing, and androgenetic alopecia.

The document concludes that there are no reliable treatments for frontal fibrosing alopecia, with only temporary benefits from current options.

A rare skin condition causes red and dark patches on the face and limbs.

A new PAX9 gene mutation causes missing teeth and hair problems, but not skin or nail issues.

Apremilast may help treat lichen planopilaris and frontal fibrosing alopecia when other treatments fail.

A patient with steroid sulfatase deficiency had a unique hair pattern and a brain malformation not previously linked to the condition.

People with the same genetic mutation for Woodhouse-Sakati syndrome can have different symptoms.

Tofacitinib successfully treated hair loss in a Crohn's disease patient who previously used adalimumab.

A 15-year-old boy's severe scalp condition improved significantly with adalimumab and baricitinib treatment.

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

A new genetic mutation linked to CARASIL syndrome and small artery disease was found in a Chinese family.

Ixekizumab may be an effective first treatment for a rare skin condition causing hair loss.

One twin girl has Loose anagen syndrome with poorly anchored hair, diagnosed with a simple hair pull test, while her identical twin does not have the condition.

A multidisciplinary approach is crucial for treating complex cases of Rapunzel syndrome in children.

Inhibiting AP-1 changes skin tumor types and affects tumor cell identity.

Tofacitinib shows promise for treating severe hair loss in adults and teens, with many experiencing regrowth, but hair loss returns when treatment stops.

A deficiency in the TTC7A gene causes immune problems, gut issues, and hair loss.

Rapunzel syndrome can show vague symptoms and needs long-term psychiatric care to prevent recurrence.

A 2-year-old girl had a hair disorder not shared by her identical twin.

A new genetic variant in the LIPH gene causes hair growth issues in a Chinese patient.

Congenital atrichia is a rare condition where children are born without hair, and treatment is often ineffective.

Get head MRI for babies with achondroplasia early, use free immunoglobulin light chains to detect certain neurodevelopmental disorders, and video calls work for speech therapy in patients with facial anomalies.

The AA-IGA scale reliably measures treatment success in alopecia areata by considering both clinician and patient views.

A genetic region near the PAX1 gene is linked to a higher risk of scoliosis in females.

Hutchinson-Gilford Progeria Syndrome caused rapid aging due to a genetic mutation, with treatments to manage symptoms.

The document concludes that a woman has both Frontal Fibrosing Alopecia and Lichen Simplex Chronicus, a previously unreported combination of conditions.

Intralesional triamcinolone acetonide helps regrow eyebrows in patients with frontal fibrosing alopecia.