Congenital Absence of the Intrahepatic Bile Ducts

Haas, Leonard A.; Dobbs, Richard H.

doi:10.1136/adc.33.171.396

Cited by 39 publications

(11 citation statements)

References 15 publications

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“…The seven cases of intrahepatic biliary atresia provide too small a group for analysis, but the absence of any familial incidence is in keeping with other reports (Ahrens, Harris and MacMahon, 1951;Haas and Dobbs, 1958); these authors add six cases to our seven.…”

Section: Discussionsupporting

confidence: 89%

A Genetic Study of Neonatal Obstructive Jaundice

Danks¹,

Bodian²

1963

Archives of Disease in Childhood

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Section: Discussionsupporting

confidence: 89%

A Genetic Study of Neonatal Obstructive Jaundice

Danks¹,

Bodian²

1963

Archives of Disease in Childhood

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“…Congenital absence of the intrahepatic bile-ducts was described by Haas and Dobbs (1958), who recorded obstructive jaundice which started in the first week of life, but improved with time. The jaundice in the present two cases increased with age.…”

mentioning

confidence: 99%

Familial intrahepatic cholestatic jaundice in infancy.

Gray¹,

Saunders²

1966

Archives of Disease in Childhood

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“…A rather similar case was reported by Sass-Kortsak et c~l.~~ and the condition has been discussed in some detail by Ahrens et all and Haas and Dobbs. 15 The two cases in Group H are of interest as we failed to find similar reports in the literature. Both infants had only fibrous rudiments of gallbladder and extra-hepatic bile ducts.…”

Section: Gross Pathologymentioning

confidence: 69%