WordNet

of or relating to infants or infancy; "infantile paralysis"
being or befitting or characteristic of an infant; "infantile games"
malignant neoplasm of blood-forming tissues; characterized by abnormal proliferation of leukocytes; one of the four major types of cancer (同)leukaemia, leucaemia, cancer of the blood

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1. 小児および思春期における急性リンパ芽球性白血病の症状および診断の概要 overview of the presentation and diagnosis of acute lymphoblastic leukemia in children and adolescents
2. 小児および思春期における急性リンパ芽球性白血病の治療の概要 overview of the treatment of acute lymphoblastic leukemia in children and adolescents
3. 小児および思春期における急性リンパ芽球性白血病の転帰に関する概要 overview of the outcome of acute lymphoblastic leukemia in children and adolescents
4. 急性骨髄性白血病の分類 classification of acute myeloid leukemia
5. 小児および思春期における急性リンパ芽球性白血病のリスクグループ層別化および予後 risk group stratification and prognosis for acute lymphoblastic leukemia in children and adolescents

Mutations of the Imprinted CDKN1C Gene as a Cause of the Overgrowth Beckwith-Wiedemann Syndrome: Clinical Spectrum and Functional Characterization.

Brioude F1,2,3, Netchine I1,2,3, Praz F1,3, Le Jule M2, Calmel C3, Lacombe D4,5, Edery P6,7, Catala M8,9, Odent S10,11, Isidor B12,13, Lyonnet S14,15, Sigaudy S16, Leheup B17,18, Audebert-Bellanger S19, Burglen L20,21, Giuliano F22, Alessandri JL23, Cormier-Daire V24,25, Laffargue F26, Blesson S27, Coupier I28, Lespinasse J29, Blanchet P30, Boute O31, Baumann C32, Polak M33,34, Doray B35, Verloes A32, Viot G36, Le Bouc Y1,2,3, Rossignol S3,35.
Human mutation.Hum Mutat.2015 Sep;36(9):894-902. doi: 10.1002/humu.22824. Epub 2015 Aug 6.
Beckwith-Wiedemann syndrome (BWS) is an imprinting disorder associating macroglossia, abdominal wall defects, visceromegaly, and a high risk of childhood tumor. Molecular anomalies are mostly epigenetic; however, mutations of CDKN1C are implicated in 8% of cases, including both sporadic and familial
PMID 26077438

Unmistakable Morphology? Infantile Malignant Osteopetrosis Resembling Juvenile Myelomonocytic Leukemia in Infants.

Strauss A1, Furlan I2, Steinmann S2, Buchholz B3, Kremens B4, Rossig C5, Corbacioglu S6, Rajagopal R7, Lahr G2, Yoshimi A8, Strahm B8, Niemeyer CM8, Schulz A2.
The Journal of pediatrics.J Pediatr.2015 Aug;167(2):486-8. doi: 10.1016/j.jpeds.2015.04.064. Epub 2015 May 15.
The initial clinical and hematologic presentation of infantile malignant osteopetrosis may be indistinguishable from that of juvenile myelomonocytic leukemia in infants. Timely radiographic imaging, however, allows straightforward delineation of these 2 severe diseases and facilitates immediate init
PMID 25982139

Neonatal acute lymphocytic leukaemia: an unusual presentation of a rare disease.

Palman J1, Karam M1, Chee Y1, Kandala V1.
BMJ case reports.BMJ Case Rep.2015 Jul 15;2015. pii: bcr2015210606. doi: 10.1136/bcr-2015-210606.
Infantile acute lymphocytic leukaemia (ALL) seldom presents within the first month of life. Most are diagnosed before birth. Postnatal diagnoses are easily recognisable when characteristic features are present, namely hepatosplenomegaly, leukaemia cutis or infiltrative disease of the extramedullar a
PMID 26178003