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Children with Parry Romberg Syndrome had successful facial fat-grafting surgeries after disease stabilization with no complications.

Male hormones and reduced plakoglobin can impair heart electrical function and increase arrhythmia risk in males.

A new method accurately measures a drug in skin for cancer therapy research.

A boy with Pachyonychia congenita has a confirmed gene mutation, highlighting the need for a local genetic database in India.

The revised BASP classification for hair loss is less accurate and harder to use but could still be a viable option.

The MAPK/ERK pathway is crucial in controlling cell growth and death in finasteride-induced hypospadias.

A new method improves platelet testing for heart disease patients.

A Chinese male with a new genetic mutation has a skin condition and severe urinary issues, with treatments having mixed success.

Claudin-1 is important for the barrier function and growth of hair.

The PEEK cage reduced pain more than the dynamic cervical implant, but the implant allowed slightly better movement after surgery.

Prolactin affects hair growth cycles and can cause early hair follicle regression.

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

The laser treatment effectively improved facial pigmentation with no major side effects.

The length of the CAG repeat in the androgen receptor gene affects the risk and progression of prostate cancer, BPH, infertility, and undermasculinized genitalia.

Some drugs can cause temporary or permanent hair loss.

Barbed sutures improve surgical outcomes and efficiency but are limited by cost and strength issues.

Hair-thread Tourniquet Syndrome, where hair or thread tightly wraps around a body part, is not rare and requires early detection to prevent serious damage.

DHT deficiency can disrupt cell connections in rat testes, possibly affecting fertility.

Taking tamsulosin or finasteride and being older increase the risk of floppy iris during cataract surgery.

Latanoprost eye drops caused excessive cheek hair growth and eyelash whitening in a woman.

Plerixafor may help treat pigmentation disorders by promoting skin repigmentation.

Combining hair transplantation with PRP is more effective for treating hair loss than hair transplantation alone.

Lhx2 is a crucial regulator of the Sonic Hedgehog signaling in early mouse retinal development.

Negative pressure treatment improved skin thickness, blood vessel growth, and hair growth.

The p.P25L mutation in the KRT5 gene causes a rare skin condition that worsens over time and may lead to hair loss starting in young adulthood.

Finasteride can reliably cause hypospadias in rabbits.

Accurate diagnosis of pseudolymphomatous folliculitis is crucial to avoid mistaking it for more serious conditions.