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A boy with chromosome 13q deletion syndrome developed eye cancer, a woman with breast cancer lost vision due to a rare side-effect of her treatment, a man's vision worsened after using a hair loss drug, and two rare disorders were discussed. Optical Coherence Tomography is useful for diagnosing and monitoring these conditions.

Björnstad syndrome causes twisted hair from birth.

Cronkhite-Canada syndrome may be more treatable and less severe than previously thought.

Long non-coding RNAs play a key role in yak hair growth cycles.

Overexpressing Merkel cell virus proteins in human hair follicles can create clusters of cells that resemble Merkel cell cancer.

NEMO syndrome and systemic lupus erythematosus are linked in a new disease association.

Cats with abnormal hair had DSG4 gene changes causing hair problems.

Higher levels of nidogen1 and type IV collagen are found in basal cell carcinoma compared to normal skin.

Hair matrix cysts are rare skin nodules with unique features, often needing surgical removal.

Cell membrane-coated nanoparticles could improve gene therapy by enhancing delivery and targeting of nucleic acids.

Netherton's disease causes multiple hair defects.

The Msx2 gene affects feather development in Hungarian white geese and a specific gene variation could indicate feather quality.

The vector successfully directed specific gene expression in hair follicles.

A new change in the WNT10A gene caused a condition leading to short hair growth in a Chinese family.

Mutations in the vitamin D receptor cause hereditary vitamin D-resistant rickets, leading to poor bone health and requiring high calcium doses for treatment.

Certain circular RNAs help cashmere goats grow more hair.

A specific RNA in cashmere goats helps improve hair growth by interacting with certain molecules.

Different long non-coding RNAs in yaks change during hair growth cycles and are involved in key growth pathways.

HOXC13 is essential for hair and nail development by regulating Foxn1.

OCT4B1 and SOX-2 levels are higher in Crohn's and ulcerative colitis patients, possibly aiding tissue repair.

PCOS involves immune and genetic factors, with key roles for T cells and specific genes.

Congenital Adrenal Hyperplasia is a rare inherited disease causing hormone imbalances, affecting growth, fertility, and heart health, diagnosed through blood tests and treated with medication and lifestyle changes.

A 10-year-old boy was diagnosed with a rare scalp condition causing hair loss and treated with a topical cream.

Early and accurate diagnosis of congenital smooth muscle hamartomas is crucial to distinguish them from other conditions.

A newborn with severe low blood sugar due to a genetic issue needed major surgery after standard treatments failed.

Sebaceous nevus changes with age, and dermoscopy and RCM are effective for diagnosis.

A new genetic tool improves the study of hair growth and potential hair disorder treatments.

The DMI3 gene is essential for nodule development and symbiosis in certain plants.

Genes linked to fibrosis are more active in people with central centrifugal cicatricial alopecia.