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| Neonatal-Onset PIGT Encephalopathy: A Rare Korean Case with Hypophosphatasia |
| Min Jun Chun, Yeon Sook Moon, Woo Ri Jang, Jong Hee Chae, Young Se Kwon |
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Ann Child Neurol. 2022;30(1):35-37. Published online September 9, 2021 DOI: https://doi.org/10.26815/acn.2021.00444 |
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Neonatal-Onset PIGT Encephalopathy: A Rare Korean Case with Hypophosphatasia Annals of Child Neurology. 2021;30(1):35-37  A case of chronic epileptic encephalopathy of neonatal onset Brain and Development. 1993;15(6):448-452 A case of neonatal peroneal neuropathy with intrauterine onset Korean Journal of Pediatrics. 2007;50(6):585 Adult-onset portosystemic encephalopathy caused by patent ductus venosus successfully treated with endovascular coil embolization: a rare case report CVIR Endovascular. 2020;3(1): Hypophosphatasia as a rare cause of neonatal seizures Archives de Pédiatrie. 2021;28(6):496-499 Case of Juvenile Onset Hypophosphatasia Diagnosed in an Adult Patient Journal of the Endocrine Society. 2021;5(Supplement_1):A187-A188 Abstract #806755: Adult Hypophosphatasia: A Rare and Underrecognized Phenomena, Case Report Endocrine Practice. 2020;26:70-71 Hypophosphatasia Orphanet Journal of Rare Diseases. 2007;2(1): Case Report of Lethal Perinatal Hypophosphatasia with Seizure and Respiratory Failure Diagnosed by ALPL Gene Mutation Neonatal Medicine. 2020;27(1):26-30 A Rare Presentation of Non-Traumatic Recurring Bone Fractures in Adult Patient With Juvenile Onset Hypophosphatasia Journal of the Endocrine Society. 2021;5(Supplement_1):A178-A178 |
