WordNet

an impairment of health or a condition of abnormal functioning
either of two bean-shaped excretory organs that filter wastes (especially urea) from the blood and excrete them and water in urine; "urine passes out of the kidney through ureters to the bladder"
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優性多発性嚢胞腎 autosomal dominant polycystic kidney disease in children
2. 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
3. 常染色体優性多発性嚢胞腎の経過および治療 course and treatment of autosomal dominant polycystic kidney disease
4. 常染色体優性多発性嚢胞腎の診断およびスクリーニング diagnosis of and screening for autosomal dominant polycystic kidney disease
5. カロリー病 caroli disease

Hypertelorism, radial ray defects, dextrocardia, hypoplastic ribs and renal anomaly: report of a second case and confirmation of the phenotype.

Fuchs GE, Suri M, Dux A, Craft EV, Vasudevan PC, Tanteles GA.SourceDepartment of Clinical Genetics, Leicester Royal Infirmary, Leicester, UK.
Clinical dysmorphology.Clin Dysmorphol.2012 Jul;21(3):157-61.
PMID 22610273

Boy with autosomal recessive polycystic kidney and autosomal dominant polycystic liver disease.

Zingg-Schenk A, Caduff J, Azzarello-Burri S, Bergmann C, Drenth JP, Neuhaus TJ.SourceChildren's Hospital Lucerne, 6000, Lucerne, Switzerland.
Pediatric nephrology (Berlin, Germany).Pediatr Nephrol.2012 Jul;27(7):1197-200. Epub 2012 Mar 14.
BACKGROUND: Autosomal recessive polycystic kidney disease (ARPKD) shows a great phenotypic variability between patients, ranging from perinatal demise to mildly affected adults. Autosomal dominant polycystic liver disease (PCLD) does not manifest in childhood. CASE-DIAGNOSIS/TREATMENT: A boy was rep
PMID 22415584

長尾静子,小山洋一,高橋久英
Experimental Animals 43(4), 511-519, 1994
我々は, マウス多発性嚢胞腎症 (PKD) における腎臓の異常を解析するために, 成人型PKDマウスであるDBA/2FG-pcyの腎臓を免疫したDBA/2マウスから得た脾臓と, P3U1ミエローマ細胞を融合し, マウスの腎臓に反応するモノクロナール抗体を作製した。得られたクローンのひとつであるD28は, DBA/2マウスとDBA/2FG-pc …
NAID 130005001164

津田浩史,今中基晴,荻田幸雄,新宅晴夫
産婦人科の進歩 44(4), 380-384, 1992
… We recently experienced a case of atypical fetal polycystic kidney disease (IPKD). … During admission, the sonographic findings for the fetus demonstrated a normal appearing bladder, oligohydramnios, bilateral hyperechoic kidney (not enlarged), and reduced fetal urine production. These findings suggested a diagnosis of atypical fetal polycystic kidney disease. …
NAID 130004069562

長尾静子,高橋久英
Experimental Animals 40(4), 557-560, 1991
一般にヒトの多発性嚢胞腎症 (PKD) の疾患モデルとして, 幼児型のcpkマウスと成人型のpcyマウスが用いられている。一方, ラットでは幼児型と成人型のPKDは, それぞれCy遺伝子のホモ型とヘテロ型に起因している。そこで, 2つのマウスPKD遺伝子が同一遺伝子の対立形質であるか否 …
NAID 130005000935