WordNet

an impairment of health or a condition of abnormal functioning
of or relating to infants or infancy; "infantile paralysis"
being or befitting or characteristic of an infant; "infantile games"
caused by or altered by or manifesting disease or pathology; "diseased tonsils"; "a morbid growth"; "pathologic tissue"; "pathological bodily processes" (同)morbid, pathologic, pathological

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1. 小児における常染色体劣性多発性嚢胞腎 autosomal recessive polycystic kidney disease in children
2. HIV関連腎症（HIVAN） hiv associated nephropathy hivan
3. 小児におけるステロイド抵抗性特発性ネフローゼ症候群 steroid resistant idiopathic nephrotic syndrome in children
4. 先天性肺気道奇形の出生前診断およびマネージメント prenatal diagnosis and management of congenital pulmonary airway malformation
5. 先天性乳児ネフローゼ症候群 congenital and infantile nephrotic syndrome

[Treatment of infantile vascular malformations associated with airway obstruction].

Liu XJ1, Qin ZP, Tai MZ, Li KL.
Zhonghua er bi yan hou tou jing wai ke za zhi = Chinese journal of otorhinolaryngology head and neck surgery.Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi.2010 Jan;45(1):32-7.
OBJECTIVE: To summarize the clinical features of vascular malformations complicated with airway obstruction and to evaluate the therapeutic methods of these disease.METHODS: Forty-seven children with airway obstruction and dyspnea (25 males, 22 females) were treated from Jun 1985 to Dec 2007, and th
PMID 20398536

Infantile chronic tubulo-interstitial nephritis with cortical microcysts: variant of nephronophthisis or new disease entity?

Gagnadoux MF1, Bacri JL, Broyer M, Habib R.
Pediatric nephrology (Berlin, Germany).Pediatr Nephrol.1989 Jan;3(1):50-5.
Over a 15-year period we observed seven children (four girls, three boys) who presented within the first months of life with severe renal failure and acidosis, associated with hypertension in five patients and polyuria in four. In addition, one patient had a severe cholestatic liver disease. In two
PMID 2702088

Peanut and Lotus tetragonolobus binding sites in human kidney from congenital nephrotic syndrome of Finnish type.

Barresi G1, Tuccari G, Arena F.
Histochemistry.Histochemistry.1988;89(2):117-20.
The authors have studied kidney tissues from two cases of Congenital Nephrotic Syndrome of Finnish Type (CNS:FT), two cases of infantile polycystic disease and five normal newborns using Peanut (PNA) and Lotus Tetragonolobus (LTA) peroxidase-labeled lectins. In CNS:FT a positive reaction for LTA has
PMID 3397305