Farber's disease type IV presenting with cholestasis and neonatal liver failure: Report of two cases

Asha Willis, Cherie Van Huse, Kimberly P. Newton, Melissa P. Wasserstein, Raffaella A. Morotti

Research output: Contribution to journalArticle

9 Citations (Scopus)

Abstract

We report 2 siblings diagnosed with Farber's disease type IV Type IV is a subtype of Farber's disease that presents in the neonatal period and usually initially lacks the triad of symptoms, including painful and deformed joints, subcutaneous nodules, and hoarse cry, classically seen in the other subtypes. While it is well known that all neonates with type IV present with hepatomegaly, a previously unrecognized presentation is that of cholestatic jaundice and rapidly evolving liver failure. We describe 2 siblings who presented with jaundice in the neonatal period and discuss the clinical data and variation in pathologic findings that should be considered for the diagnosis.

Original languageEnglish (US)
Pages (from-to)305-308
Number of pages4
JournalPediatric and Developmental Pathology
Volume11
Issue number4
DOIs
StatePublished - Jul 2008
Externally publishedYes

Fingerprint

Farber Lipogranulomatosis
Cholestasis
Liver Failure
Neonatal Jaundice
Hepatomegaly
Obstructive Jaundice
Joints

Keywords

  • Farber type IV
  • Liver failure
  • Neonatal cholestasis

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health
  • Pathology and Forensic Medicine

Cite this

Farber's disease type IV presenting with cholestasis and neonatal liver failure : Report of two cases. / Willis, Asha; Van Huse, Cherie; Newton, Kimberly P.; Wasserstein, Melissa P.; Morotti, Raffaella A.

In: Pediatric and Developmental Pathology, Vol. 11, No. 4, 07.2008, p. 305-308.

Research output: Contribution to journalArticle

Willis, Asha ; Van Huse, Cherie ; Newton, Kimberly P. ; Wasserstein, Melissa P. ; Morotti, Raffaella A. / Farber's disease type IV presenting with cholestasis and neonatal liver failure : Report of two cases. In: Pediatric and Developmental Pathology. 2008 ; Vol. 11, No. 4. pp. 305-308.
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