The Indian Journal of Pediatrics

, Volume 69, Issue 9, pp 825–827 | Cite as

Alagille syndrome

  • Harshalee Shendge
  • Milind S. Tullu
  • Asha Shenoy
  • Rachana Chaturvedi
  • Jaishree R. Kamat
  • Manisha Khare
  • Amita Joshi
Clinical Brief

Abstract

Syndromic paucity of bile ducts or “Alagille syndrome” is characterized by peculiar facies, chronic cholestasis, posterior embryotoxon, butterfly-like vertebral arch defects and peripheral pulmonary artery hypopiasia or stenosis. We present a two-year-old female child with the ‘partial’ or ‘incomplete’ Alagille syndrome. The child had three of the five major features of the syndrome. A brief review of literature of the syndrome is presented.

Key words

Artehohepatic dysplasia Bilirubin Cholestasis Embryotoxon Pulmonary stenosis Vertebral defects 

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Copyright information

© Dr. K C Chaudhuri Foundation 2002

Authors and Affiliations

  • Harshalee Shendge
    • 2
  • Milind S. Tullu
    • 2
  • Asha Shenoy
    • 1
  • Rachana Chaturvedi
    • 1
  • Jaishree R. Kamat
    • 2
  • Manisha Khare
    • 1
  • Amita Joshi
    • 1
  1. 1.Departments of PathologySeth G. S. Medical College and KEM HospitalMaharashtraIndia
  2. 2.Departments of PediatricsSeth G. S. Medical College and KEM HospitalMaharashtraIndia

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