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Newborn screening and gene therapy are expected to improve outcomes for Omenn syndrome patients.

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

Sardinians were historically short due to a mix of genetics and factors like disease and poor nutrition, but recent height increases suggest better living conditions had a bigger impact.

Proper nutrition can help manage PCOS symptoms and improve overall health.

Bariatric surgery affects skin health, causing both direct complications and changes in existing skin conditions, often related to nutritional deficiencies.

Genetics and nutritional deficiencies are key factors in premature graying of hair.

Rural Bangladeshi girls mature later than peers in other low and middle-income countries due to poor nutrition and socioeconomic conditions.

Choline and biotin are important for liver health and preventing certain deficiencies in animals, and more research is needed to understand their benefits in humans.

Childhood obesity is rising globally due to various factors, and early prevention and healthy lifestyle changes are crucial.

European guidelines recommend regular eye and ear exams, skin care, vitamin D supplements, and cautious use of medications for managing congenital ichthyoses.

Men with a family history of hair loss are more likely to experience it themselves, especially if both parents have hair loss.

The spiny mouse is a unique menstruating rodent that can help us understand menstruation and reproductive disorders.

The document concludes that changes in eyelashes and eyelid skin can indicate various local and systemic diseases.

Chemotherapy in children often causes hair loss, nausea, vomiting, and mood swings.

An 11-year-old child with total hair loss may have a genetic autoimmune disease, and the outlook for hair regrowth is not good.

Anorexia and bulimia lead to serious health problems and increased risk of death, requiring aggressive treatment.

Liver transplantation is a viable option for children with propionic acidemia, improving quality of life and diet, but does not remove all risks and long-term brain outcomes are uncertain.

The document reports findings on genetic research, including ethical concerns about genome editing, improved diagnosis of mitochondrial mutations, solving inherited eye diseases, confirming gene roles in epilepsy, linking a gene to aneurysms, and identifying genes associated with age-related macular degeneration.

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.

Low-dose flutamide-metformin therapy effectively improved PCOS symptoms in adolescent girls.

Chemotherapy causes hair loss by damaging hair follicles and stem cells, with more research needed for prevention and treatment.

Hair elemental analysis could be useful for health and exposure assessment but requires more standardization and research.

The most common skin problems in Indian children are infections and eczemas.

Researchers found 71 genetic regions linked to male pattern baldness, which account for 38% of its genetic risk.

Kids with early graying hair often have low levels of calcium, ferritin, and vitamin D3.

PCOS is a complex disorder managed by treating symptoms and requires a team of specialists.

The technique allowed noninvasive tracking of hair stem cell survival and growth, showing potential for hair loss research.

Children's skin diseases and treatments differ from adults and require specific approaches.

Animal research has greatly advanced dermatology.

Treating alopecia areata is difficult due to limited approved treatments, but new therapies like JAK inhibitors show promise.