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A new syndrome was linked to two new genetic changes in the MBTPS1 gene in a 14-year-old girl.

The QuantAnts machines can find cancer markers and create CRISPR targets for them.

Continued ritlecitinib treatment helps sustain hair regrowth in alopecia areata patients.

Spironolactone helps reduce fluid in the eye in Central Serous Chorioretinopathy, but doesn't improve vision and recurrence is common.

A new mutation in the FLCN gene linked to Birt-Hogg-Dube syndrome was found, suggesting people with certain lung collapse should be tested for this mutation and screened for kidney and colon cancer.

Bmpr2 and Acvr2a receptors are crucial for hair retention and color.

Vitamin D Dependent Rickets Type-2A can cause complete hair loss and bone growth issues in infants.

Keratoacanthoma changes as it grows, showing different hair follicle characteristics at each stage.

A woman with lymphoma had a rare skin rash on her scalp and forehead, which was hard to diagnose but responded well to treatment.

Photobiomodulation therapy may speed up hair regrowth after chemotherapy in the short term.

Phosphatidylinositol 4-kinases are crucial for root growth, defense, and immunity in Arabidopsis thaliana.

Immune checkpoint inhibitors can increase the risk of autoimmune skin diseases, especially bullous pemphigoid.

All-trans retinoic acid helps amelanotic melanocytes in hair follicles develop and produce pigment while reducing their growth.

Ritlecitinib is effective and safe for long-term treatment of alopecia areata.

A 5-year-old girl has lipoid proteinosis, causing voice issues, hair thinning, skin lesions, and tongue movement problems.

Keratin 17 gene mutations cause both steatocystoma multiplex and pachyonychia congenita type 2.

Ritlecitinib is effective and safe for treating severe alopecia areata, showing significant hair regrowth and improved mental health.

Ritlecitinib improves hair regrowth in alopecia areata without increasing adverse risks.

Genetic testing confirmed a young girl has Atrichia with Papular Lesions due to mutations in the hairless gene.

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

Three siblings with a genetic form of rickets showed different symptoms of the disease.

A3B5 can reduce skin pigmentation and slow melanoma growth.

Upadacitinib may help regrow hair in children with alopecia areata and is generally safe.

KRT17 may be a new target for endometrial cancer treatment because it helps cancer cells move and form new blood vessels.

Recent advances show zebrafish can model anemia, Alx4 affects craniofacial and hair development, and mTORC1 is crucial for retinal development.

Mice without certain skin enzymes have faster hair growth and bigger eye glands.

Cortisol increases a specific protein in bone cells, which may help explain its negative effects on bone.