WordNet

of or relating to or resembling a calyx (同)calycine, calycinal
a condition in which the ends of toes and fingers become wide and thick; a symptom of heart or lung disease

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1. 爪疾患の概要 overview of nail disorders
2. 間質性肺疾患を有する成人に対するアプローチ：臨床的評価 approach to the adult with interstitial lung disease clinical evaluation
3. サルコイド：筋肉、骨、血管の疾患の徴候 sarcoid muscle bone and vascular disease manifestations
4. 悪性腫瘍およびリウマチ性疾患 malignancy and rheumatic disorders
5. 胎児水腎症の概要 overview of antenatal hydronephrosis

Renal involvement in the Laurence-Moon-Bardet-Biedl syndrome: report of five cases.

Uçar B, Yakut A, Kural N, Büyükaşik F, Vardareli E.SourceOsmangazi University, Faculty of Medicine, Department of Pediatrics, Eskişehir, Turkey.
Pediatric nephrology (Berlin, Germany).Pediatr Nephrol.1997 Feb;11(1):31-5.
We report five patients with Laurence-Moon-Bardet-Biedl syndrome (LMBBS) who had renal involvement. Intravenous pyelography showed bilateral or unilateral calyceal clubbing and blunting in all patients. In addition, one patient had a parapelvic cyst in the left kidney and another had bilateral lobul
PMID 9035169

The importance of renal impairment in the natural history of Bardet-Biedl syndrome.

O'Dea D, Parfrey PS, Harnett JD, Hefferton D, Cramer BC, Green J.SourceDivision of Nephrology, Memorial University, St John's, Newfoundland, Canada.
American journal of kidney diseases : the official journal of the National Kidney Foundation.Am J Kidney Dis.1996 Jun;27(6):776-83.
Bardet-Biedl syndrome is a rare autosomal recessive disease characterized by dysphormic extremities, retinal dystrophy, obesity, hypogenitalism in males, and renal structural abnormalities. Because the clinical outcome of these patients is not well known, 21 families with Bardet-Biedl syndrome (BBS)
PMID 8651240

De Marchi S, Cecchin E, Bartoli E.SourceDepartment of Internal Medicine, University of Udine Medical School, Italy.
Renal failure.Ren Fail.1992;14(4):587-90.
An unusual association of Bardet-Biedl syndrome with cystinuria was described in one patient. A 21-year-old male was admitted to hospital because of renal failure, severe deterioration of visual acuity, polydactyly, brachydactyly, and mental retardation. Laboratory investigations revealed a serum cr
PMID 1462012

近田龍一郎,折笠精一,坂井清英,太田章三,久慈了,庵谷尚正,中道五郎
日本泌尿器科學會雜誌 80(6), 884-890, 1989-06-20
… 腎scarを認めたのは271腎中158腎58%であった.IVPとDMSA腎シンチグラムの各所見を比較すると,両者が一致したのは52%にすぎず,IVPで正常所見を示した例の41%にDMSA腎シンチグラムでscarが認められた.また,IVPで腎杯のclubbingのみを認めた例の28%,部分的な腎皮質の非薄化を認めた例の60%は,DMSA腎シンチグラムでみると腎全体に及ぶ高度のscarを伴っていた.各症例を年齢により3歳以下,4歳以上の2群にわけた場合,scarの発生率はそれぞれ …
NAID 110003084099