小児科
Pediatrics
Pediatrics
Introduction
At the Pediatrics Department of Iseikai International General Hospital, we accept consultations regarding all pediatric diseases from newborns to graduating from junior high school. We also focus on the areas of developmental support and health promotion through infant health checkups and vaccinations, and we also work on rare and intractable diseases (see the page on the Intractable Disease Medical Promotion Center for details). Children who require hospitalization can be treated in a pediatric ward. We hope that medical professionals will feel free to consult with us.
Characteristics of this department
Pediatric diseases that can be treated
All pediatric diseases from newborns to third-year junior high school students
- We also treat pediatric rheumatic diseases such as persistent fever and pain of unknown cause in general and external examinations.
- We treat short stature, obesity, and secondary examination of school urine tests.
- We provide highly specialized treatment for pediatric endocrine diseases, kidney diseases, bone diseases, etc.
- We have outpatient appointment slots for developmental health checkups and vaccinations.
We can also provide consultations on radiological tests (CT, MRI & MRA, SPECT, PET-CT).
For pediatric surgical diseases, some are treatable and some are difficult, so please consult us individually.
We have a ward that operates as a pediatric center.
It has a total of 20 beds, including 12 private rooms and 8 total rooms, and hospitalization with an attendant is possible.
Main diseases
Pediatric Diseases
Febrile convulsions, croup, asthmatic bronchitis, acetonemia, infectious gastroenteritis, gastroduodenal ulcers, cellulitis, Kawasaki disease, IgA vasculitis, nephrotic syndrome, childhood diabetes, juvenile idiopathic arthritis, familial Mediterranean fever, BCG lymphadenitis, etc.
Congenital Metabolic Disorders
Glycogen storage disease, lysosomal storage disorders (Gaucher disease, Pompe disease, Fabry disease, mucopolysaccharidosis, Krabbe disease, etc.), neurodegenerative metabolic disorders, conditions screened by newborn mass screening, mitochondrial diseases, adrenoleukodystrophy, citrin deficiency
Endocrine Disorders
Congenital hypothyroidism, growth hormone deficiency (short stature), idiopathic hypoparathyroidism, overgrowth syndromes, Sotos syndrome, Noonan syndrome, MCT8 deficiency (Allan–Herndon–Dudley syndrome), pseudohypoparathyroidism, type 1 diabetes mellitus, progeria
Bone Disorders
Osteogenesis imperfecta, achondroplasia, hypophosphatasia, X-linked hypophosphatemic rickets/osteomalacia, hypochondroplasia, McCune–Albright syndrome, Morquio syndrome
Treatment
Infusion therapy, antibiotic therapy, immunosuppressant therapy, biological therapy, etc.
Outpatient schedule
Morning 9:00～12:00（Reception8:00-11:30）/
Afternoon to Evening 13:30～16:30（Reception13:00-16:00）
| Mon | Tue | Wed | Thurs | Fri | |
|---|---|---|---|---|---|
| Morning | ● | ● | ● | ● | ● |
| Afternoon to Evening | ● | ● | ● | ● | ● |
Pediatrics Check-up and Vaccination
| Mon | Tue | Wed | Thurs | Fri | |
|---|---|---|---|---|---|
| Morning | - | - | - | - | - |
| Afternoon to Evening | - | ● | ● | - | ● |
Medical track record of the clinical department
-
Disease classification Number of patients (people) Infectious diseases 183 Bone system diseases 140 Congenital metabolic disorders 101 Other 91 Neonatal diseases 61 Endocrine diseases 49 Vaccines/examinations 40 Surgical diseases 39 Details of intractable and rare diseases
- Bone system diseases
- Endocrine Diseases
- Congenital Metabolic Disorders (Lysosomal Diseases)
- Congenital Metabolic Disorders (Other)
-
Number of patients (people) Osteogenesis imperfecta 34 Achondroplasia 41 Hypochondroplasia 6 Hypophosphatasia 13 X-linked hypophosphatemic rickets 6 Type II collagen dysplasia 6 Punctate chondrodysplasia 4 Cleidocranial dysplasia 3 Pseudoachondroplasia 2 Transformative osteodysplasia 1 Kamurati-Engelmann syndrome 1 Other 23 Total 140 -
Number of patients (people) Type 1 Diabetes 6 Sotos Syndrome 5 McCune-Albright Syndrome 4 Prader-Willi Syndrome 3 22q11.2 Deletion Syndrome 2 Down Syndrome 2 Noonan Syndrome 2 Progeria (Hutchinson-Gilford Syndrome) 2 Pseudohypoparathyroidism 1 X-linked Hypophosphatemic Rickets 1 Congenital Lipodystrophy 1 Weaver Syndrome 1 Gitelman Syndrome 1 Others 118 Total 49 -
Number of patients (people) Fabry Disease 19 Gaucher Disease 13 Pompe Disease 8 Krabbe Disease 7 Metachromatic Leukodystrophy (MLD) 4 Mucopolysaccharidosis Type II / Hunter Syndrome (MPS II) 3 Mucopolysaccharidosis Type I / Hurler Syndrome (MPS I) 2 Niemann-Pick Disease Type C2 (NPC2) 2 I-cell Disease 1 Mucopolysaccharidosis Type IV / Morquio Syndrome (MPS IV) 1 Galactosialidosis 1 GM1 Gangliosidosis 1 GM2 Gangliosidosis 1 Total 63 -
Number of patients (people) MCAD Deficiency 4 PKU (Phenylketonuria) 4 GSD Ia (Glycogen Storage Disease Type Ia) 4 GSD IX (Glycogen Storage Disease Type IX) 4 Mitochondrial Disease 4 ALD (Adrenoleukodystrophy) 3 VLCAD Deficiency 2 OTC Deficiency 2 Citrullinemia 2 Hyperornithinemia-Hyperammonemia-Homocitrullinuria Syndrome 2 Wilson Disease 1 GSD III (Glycogen Storage Disease Type III) 1 GSD VI（Glycogen Storage Disease Type VI） 1 MyD (Muscular Dystrophy - unspecified) 1 MMA (Methylmalonic Acidemia) 1 PDHC Deficiency 1 CPT2 Deficiency 1 Total 38
-
Disease classification Number of patients (people) Infectious diseases 64 Bone system diseases 18 Congenital metabolic disorders 8 Neonatal diseases 6 Endocrine diseases 2 Surgical diseases 2 Others 14
Regarding clinical research
Click here for more information on clinical research