Publications by authors named "M Ikeno"

Chondroitin, a class of glycosaminoglycan polysaccharides, is found as proteoglycans in the extracellular matrix, plays a crucial role in tissue morphogenesis during development and axonal regeneration. Ingestion of chondroitin prolongs the lifespan of C. elegans.

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Article Synopsis
  • Adenovirus is a significant cause of febrile illness and can lead to serious conditions like encephalitis/encephalopathy in children, prompting a study on its clinical features in Japan.
  • A nationwide survey collected data on children diagnosed with adenovirus-associated encephalitis/encephalopathy (AdVE) from January 2014 to March 2019, revealing demographic and clinical details, including outcomes.
  • The findings indicated that previous febrile seizures were common, with a mixed prognosis; a subset of patients had poor outcomes associated with certain laboratory markers, and different encephalopathy subtypes existed among affected children.
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The frequency of split cord malformation (SCM) is approximately 1 in 5000 births; however, patients are rarely diagnosed with SCM in the neonatal period. Moreover, there have been no reports of SCM with hypoplasia of the lower extremities at birth. A 3-day-old girl was transferred to our hospital for a thorough examination of hypoplasia of the left lower extremity and lumbosacral abnormalities detected after birth.

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Long-term peritoneal dialysis (PD) is often associated with peritoneal dysfunction leading to withdrawal from PD. The characteristic pathologic features of peritoneal dysfunction are widely attributed to peritoneal fibrosis and angiogenesis. The detailed mechanisms remain unclear, and treatment targets in clinical settings have yet to be identified.

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We report clinical and molecular findings in three Japanese patients with N-acetylneuraminic acid synthetase-congenital disorder of glycosylation (NANS-CDG). Patient 1 exhibited a unique constellation of clinical features including marked hydrocephalus, spondyloepimetaphyseal dysplasia (SEMD), and thrombocytopenia which is comparable to that of an infant reported by Faye-Peterson et al., whereas patients 2 and 3 showed Camera-Genevieve type SMED with intellectual/developmental disability which is currently known as the sole disease name for NANS-CDG.

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