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Differences in androgen receptor expression and tissue properties may lead to higher cryptorchidism risk in certain rats.

Different species use the same genes for tooth regeneration.

Genetic testing for hairless gene mutations is crucial to correctly diagnose and treat atrichia with papular lesions.

A 47-year-old man's eyelid swelling didn't improve with basic treatments, so a biopsy was needed.

Consider NF1 in newborns with rare congenital anomalies.

5% hydroxyapatite in scaffolds improves bone tissue formation and mechanical properties.

Rathke’s cleft cysts can rarely cause Cushing disease, and surgery can improve symptoms.

Naked-mouse hair lacks certain proteins and has less soluble fibril.

PHAs are promising biodegradable materials for medical and dental uses.

Severe vitamin deficiencies in children can cause significant hair problems.

Focal palmoplantar callosities may help diagnose non-Herlitz junctional epidermolysis bullosa.

Msx and Dlx genes are crucial for development, controlling cell behaviors like growth and differentiation through their roles as gene regulators.

A new mutation in the ST14 gene was found in a patient with ARIH syndrome, showing milder symptoms and no tooth issues.

Surgical removal of abnormal fat pads fixed the woman's eyelid issue caused by likely silicone injections.

Acne is a chronic disease linked to various systemic conditions and has significant psychological and social effects.

A rare ITGB6 gene variant causes intellectual disability, hair loss, and dental issues.

Uncombable hair is inherited dominantly with complete penetrance.

A 12-year-old girl was diagnosed with monilethrix, a genetic condition causing fragile, beaded hair that breaks easily, with no effective treatment available.

If someone has scaly skin, muscle stiffness, and intellectual disability, doctors should consider Sjogren-Larsson Syndrome, but other conditions if more symptoms are present.

A specific DNA duplication in Polish chickens affects feather shape by altering gene expression.

Hoxc13 is important for hair and tongue development by controlling hair keratin genes.

The term "Porokeratotic Adnexal Ostial Nevus" is suggested as a more appropriate name.

Netherton Syndrome is a non-treatable genetic disorder in children causing skin, hair, and allergy issues.

Janus kinase inhibitors may effectively treat resistant scalp conditions like folliculitis decalvans and dissecting cellulitis.

Joint replacement surgery normalized high alkaline phosphatase levels in a patient with severe osteoarthritis.

A child has a rare hair and skin disorder due to specific gene variants, suggesting broader genetic testing is needed.

The absence of functional sebaceous glands causes hair follicle destruction and scarring alopecia.

The girl's unexpected pubic hair growth led to a diagnosis different from complete androgen insensitivity syndrome.