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This case report describes a 22-year-old female with pseudoglucagonoma syndrome, where necrolytic migratory erythema resolved after treatment with topical steroids, emollients, and intravenous protein infusions, despite normal glucagon levels and absence of a glucagon-secreting tumor.

In this study, the prevalence of skin changes in hospitalized children with acute illness, categorized by nutritional status, was lower than previously reported, and the SKORDoK tool was less reliable for dermatological assessment using photographs.

In this study, a dietary protein deficiency was identified as the cause of alopecia and weight loss in captive western lowland gorillas, and protein supplementation improved their condition.

This report presents two cases of Berardinelli–Seip syndrome, emphasizing the role of genetic analysis and comprehensive care in managing the variability and complications of this rare condition.

This review discusses the similarities between myotonic dystrophy and aging, highlighting the role of cellular senescence in its pathophysiology, and reports no new clinical findings; the authors note potential anti-aging therapy applications.

In this study, a syndrome of zinc deficiency was observed in adults receiving intravenous feeding, with zinc supplementation improving symptoms except for delayed hair regrowth.

This review discusses long-term health impacts and physiological disruptions experienced by COVID-19 survivors, highlighting the potential of nutritional interventions to manage post-acute sequelae and metabolic complications.

This case report describes a 17-month-old girl with a history of itching skin, hair thinning, swelling, growth delay, anemia, and protein deficiency amidst potential food allergies and other health issues.

In this study, a novel DCAF17 gene mutation was identified in a Chinese family, suggesting a potential role in pancreatic β cell dysfunction and diabetes development in Woodhouse-Sakati syndrome.

This article describes subclinical ketosis in pregnant cows and associates it with several metabolic changes and clinical signs, reporting decreased levels of hemoglobin and glucose and increased ketone bodies.

This article reviews inherited mineral and trace element disturbances and reports no clinical results; it highlights conditions like hypomagnesaemia and acrodermatitis enteropathica linked to impaired nutrient absorption.

This study found that adding zinc to the drinking water improved hair coat and skin condition in moustached marmosets with symptoms resembling zinc deficiency.

This review discusses the link between nutritional deficiencies and cutaneous diseases, outlining risk factors, disease presentations, diagnostic processes, and supplementation in undernourished patients, but reports no new results.

This study observed a new skin disease in farmed mink in Canada, suggesting that an unidentified infectious agent, in association with secondary bacterial infection, may cause the condition.

In this case report, a 12-year-old girl with underlying sickle-thalassemia and familial stress presented with Rapunzel syndrome, a rare gastric trichobezoar, causing generalized swelling and severe anemia, which improved after surgical intervention and multidisciplinary care.

This case report describes a 4-month-old child with symptoms suggesting multiple carboxylase deficiency, which responded well to biotin therapy, highlighting the importance of early diagnosis and treatment to prevent serious health issues in infants with similar unexplained metabolic acidosis and symptoms.

This case report from Darmasaba Village, Bali, identified Colisepticemia in a 27-day-old chicken, based on clinical signs, pathology, and laboratory tests, and highlighted the need for improved farm hygiene and sanitation to prevent disease spread.

This case report describes a weaning infant diagnosed with Brandt syndrome displaying periorificial dermatitis and rapid symptom improvement following zinc supplementation.

This case report describes a rare instance where a child with nonketotic hyperglycinemia developed an acrodermatitis enteropathica-like eruption, likely due to combined zinc and branched chain amino acid deficiencies.

This case report describes the occurrence of juvenile diabetes mellitus with concurrent exocrine pancreatic insufficiency in a Thai Bangkaew dog, highlighting its successful management with insulin, pancreatic enzymes, and methylcobalamin.

This study found that different doses of methionine altered the composition of developing tooth germs in newborn rats, with incisor and molar germs affected differently but no statistical difference in body weight.

This study found that male rats on a riboflavin-deficient diet gained significantly less weight and developed symptoms such as alopecia and dermatitis compared to control rats receiving riboflavin.

This study suggests that myotonic dystrophies may qualify as segmental progeroid disorders due to molecular and clinical similarities with typical progeroid syndromes.

In this study, bezafibrate treatment improved certain aging-like features in a mouse model with mitochondrial dysfunction, but did not enhance muscle function or lifespan.

Neuromyotonia and morphoea can occur together in the same body areas.

This study found that maternal sub-maintenance nutrition reduced the density and branching ratio of secondary wool follicles in Merino sheep fetuses and identified genes potentially involved in these processes.

In this case study, a man with necrolytic migratory erythema and a glucagonoma experienced decreased plasma glucagon levels and reduced metastases after treatment with dimethyltriazenoimidazole carboxamide.

This case report describes a patient with adrenomyeloneuropathy, highlighting unusual MRI findings of high signal areas in the right striatum.

This study found that most milk powder samples tested from the Romanian market contained element concentrations exceeding legal limits, especially potassium, calcium, chlorine, phosphorus, and aluminum.

This study reported that mice on a phenylalanine-deficient diet showed symptoms such as weight loss, gastric dilation, and thymic depletion, which echo human phenylalanine deficiency manifestations.