Familial achalasia in children

Fawaz Chikh Torab, Moustafa Hamchou, Gabriel Ionescu, Ahmed H. Al-Salem

Research output: Contribution to journalArticlepeer-review

13 Citations (Scopus)

Abstract

Achalasia is rare in the pediatric age group and in most cases it is idiopathic with no family history. Familial achalasia is very rare. This report describes two families with achalasia: in one, six children were affected while in the other a brother and a sister had Allgrove's syndrome (triple-A syndrome consisting of achalasia, adrenal insufficiency, and alacrima). Familial achalasia suggests that it is hereditary and may be transmitted as an autosomal recessive trait. The management of achalasia in children is still controversial. With the recent advances in minimal invasive surgery, laparoscopic Heller's myotomy is the procedure of choice in the management of achalasia in children.

Original languageEnglish
Pages (from-to)1229-1233
Number of pages5
JournalPediatric Surgery International
Volume28
Issue number12
DOIs
Publication statusPublished - Dec 1 2012

Keywords

  • Achalasia
  • Children
  • Familial
  • Heller's myotomy
  • Hereditary

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health
  • Surgery

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