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SACUMAN, a rare condition causing hair loss without clear signs, is often misdiagnosed and needs scalp biopsies for accurate detection.

Infant baboons suffered from zinc poisoning due to poor cage conditions.

Low selenium levels worsen health but increase lifespan in mice.

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.

Enzyme replacement therapy may help alleviate symptoms in complex cases like this.

A man's skin condition and poor diet led to a scurvy diagnosis.

Zinc is crucial for growth and health in rats.

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Altering SSAT affects fat metabolism and body fat in mice.

Calves need enough riboflavin for healthy growth and development.

Both Egyptian and Omani obese men share similar obesity-related factors, emphasizing the need for healthy eating and exercise.

Children with severe ichthyosis and growth failure rarely have nutritional deficiencies or gastrointestinal issues, but may experience chronic dehydration.

The treatment with valproate, acetylcarnitine, folic acid, and vitamin B12 may improve muscle strength in children with SMA without significant side effects.

Monilethrix is not caused by a metabolic defect.

Magnesium deficiency raises diastolic blood pressure and reduces vascular contraction.

Kennedy's disease leads to muscle weakness and sensory issues, has no cure but manageable symptoms, and future treatments look promising.

Iron deficiency can cause fatigue, exercise intolerance, and cognitive issues, even without anemia.

A fungal infection caused skin lesions in farmed mink kits, but they remained healthy.

A new MBTPS2 gene variant disrupts fat metabolism and collagen production, causing Osteogenesis imperfecta.

Cattle in Mymensingh, Bangladesh, face high parasitic disease rates, needing better deworming and management.

A rare genetic mutation causes Woodhouse-Sakati syndrome symptoms.

Not having the gene PLAAT3 leads to fat loss, high insulin resistance, and abnormal fat levels in the blood due to a disruption in fat cell development and function.

Biotinidase deficiency can mimic other conditions, making early diagnosis and treatment crucial to prevent lasting issues.

A new mutation in the HR gene causes hair loss in a specific family.

Cronkhite-Canada syndrome is rare, with high mortality and cancer risk, needing more research for treatment guidelines.

Eating fewer calories may slow skin aging and improve skin health through various biological changes.

A child died from eating hair, causing severe stomach blockages and infection.

Improving cage hygiene and sanitation is crucial to prevent colisepticemia in chickens.

Thyroid hormone therapy effectively treated the man's rare muscle and heart issues.

Telogen Effluvium is a condition causing excessive hair loss due to stress, illness, drugs, or hormonal changes, and can be treated with specific products or naturally resolves after 3-4 years.