Page 39 - Abstract Book KONIKA 18

Syndrome: A Case Report 310
P–NMD–003 Outcomes of Acute Lymphoblastic Leukemia Children with Malnutrition
(Prime in Prof. DR. R. D. Kandou Hospital Manado 311
e-Poster)

P–NMD–004 Heterozygous Pathogenic Mutation in PLA2G6 Gene causing Infantile
Neuroaxonal Dystrophy in 2-year-old Girl: Case Report 311

P–NMD–005 Characteristics of Pediatric Patients with Severe Malnutrition at Jailolo
General Hospital 312
P–NMD–006 Marasmic Type Protein Energy Malnutrition with Hydranencephaly
and Cerebral Palsy in An 8-year-5-month-old Girl 312

P–NMD–007 Obesity in A 13-year-old boy with Periodic Paralysis Hypokalemia 313
P–NMD–008 Nutritional Status and Associated Factors in Pediatric Patients
at RSUP Dr. M. Djamil Padang 313
P–NMD–009 Primary Hypertrigliceridemia in Children with Familial Chylomicronemia
Syndrome: A Case Report 314

P–NMD–010 Respiratory Problem in A Child with Late-Onset Pompe Disease:
Frst Case in Indonesia 314

P–NMD–011 Type III B Mucopolysaccharidosis in A 14-year-old Girl: A Case Report 315
P–NMD–012 X-linked Adrenoleukodystrophy in A 10-year-old Boy 315

P–NMD–013 Diet and Physical Activity of Adolescent Nutritional Status
at SMPN 10 Cimahi City 316
P–NMD–014 X-linked Adrenoleukodystrophy: A Case Report in A Child with Typical
Clinical Features 316
P–NMD–015 Ketogenic Diet for Drug Resistant Epilepsy in Children: A Case Series 317
P–NMD–016 The Anthropometric Status among Pediatric Patients with Transfusion-
dependent Beta-thalassemia in Ulin Hospital, Banjarmasin 317
P–NMD–017 Characteristics of Patients with Enteral Nutrition Support at Nutrition
and Metabolic Disease Outpatient Clinic in Harapan Kita National
Women and Children Hospital 318
P–NMD–018 PLA2G6-Associated Neurodegeneration: An Ultra-Rare Case
of Neurodegeneration with Brain Iron Accumulation in a Child 318
P–NMD–019 Marasmus and Stunting in A 7-month-old Girl with Sepsis, Community
Acquired Pneumonia, Epilepsy, Microcephaly, and Craniosynostosis 319

P–NMD–020 A Rare Case of Joubert Syndrome 319
P–NMD–021 Leigh Syndrome with SURF1 Gene Mutation in A 7-year-9-month-old
Boy: A Case Report 320
P–NMD–022 Case Report of Two Patients with Mucopolysaccaharidoses Type II
(Hunter Syndrome) in Haji Adam Malik General Hospital 320

P–NMD–023 Outcomes of Critically Ill Children with Malnutrition in Pediatric Intensive

KONIKA XVIII Abstract Book xxxix