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Literature DB >> 9377141

Neonatal presentation of Caroli's disease.

F Keane¹, N Hadzić, M L Wilkinson, S Qureshi, C Reid, A J Baker, G Mieli-Vergani.

Abstract

A neonatal presentation of Caroli's disease with severe cardiac and progressive renal pathology is described. The availability of small paediatric endoscopes ensured early diagnosis. Despite aggressive medical management, the baby died with severe bleeding complications before potentially life saving multiple organ transplantation could take place.

Entities: Disease

Mesh：

Year: 1997 PMID： 9377141 PMCID： PMC1720696 DOI： 10.1136/fn.77.2.f145

Source DB: PubMed Journal: Arch Dis Child Fetal Neonatal Ed ISSN： 1359-2998 Impact factor: 5.747

5 in total

1. [Congenital polycystic dilation of the intrahepatic bile ducts; attempt at classification].

Authors: J CAROLI; R SOUPAULT; J KOSSAKOWSKI; L PLOCKER
Journal: Sem Hop Date: 1958-02-18

2. Refining the map and defining flanking markers of the gene for autosomal recessive polycystic kidney disease on chromosome 6p21.1-p12.

Authors: G Mücher; B Wirth; K Zerres
Journal: Am J Hum Genet Date: 1994-12 Impact factor: 11.025

Review 3. Biliary tract disease in children.

Authors: C F McEvoy; F J Suchy
Journal: Pediatr Clin North Am Date: 1996-02 Impact factor: 3.278

4. Hepatobiliary fibropolycystic diseases. A clinical and histological review of 51 patients.

Authors: J A Summerfield; Y Nagafuchi; S Sherlock; J Cadafalch; P J Scheuer
Journal: J Hepatol Date: 1986 Impact factor: 25.083

5. Endoscopic retrograde cholangiopancreatography in infantile cholestasis.

Authors: M L Wilkinson; G Mieli-Vergani; C Ball; B Portmann; A P Mowat
Journal: Arch Dis Child Date: 1991-01 Impact factor: 3.791

5 in total

7 in total

Neonatal presentation of Caroli's disease.

1. [Congenital polycystic dilation of the intrahepatic bile ducts; attempt at classification].

2. Refining the map and defining flanking markers of the gene for autosomal recessive polycystic kidney disease on chromosome 6p21.1-p12.

Review 3. Biliary tract disease in children.

4. Hepatobiliary fibropolycystic diseases. A clinical and histological review of 51 patients.

5. Endoscopic retrograde cholangiopancreatography in infantile cholestasis.

Review 1. Congenital hepatic fibrosis and autosomal recessive polycystic kidney disease.

Review 2. Choledochal cysts: part 1 of 3: classification and pathogenesis.

3. Hilar Fibropolycystic Liver Disease of Unknown Etiology: A Revelation from the Explant Liver.

Review 4. Caroli's disease: identification and treatment strategy.

5. Whole exome sequencing identifies recessive PKHD1 mutations in a Chinese twin family with Caroli disease.

6. Caroli's disease: Description of a case with a benign clinical course.

7. Factors contributing to diagnostic delay of Caroli syndrome: a single-center, retrospective study.