Literature DB >> 9475097

Familial persistent pulmonary hypertension of the newborn resulting from misalignment of the pulmonary vessels (congenital alveolar capillary dysplasia).

H B Vassal1, M Malone, A J Petros, R M Winter.   

Abstract

Misalignment of the pulmonary veins with congenital alveolar capillary dysplasia, although rare, has been reported as a cause of persistent pulmonary hypertension of the newborn. Reported cases have been mainly sporadic. Familial occurrence has been reported in only three instances. We present affected sibs with this condition. In addition to pulmonary abnormalities, urogenital abnormalities, including ureteric and urethral obstruction, seem to be common. Autosomal recessive inheritance is suggested.

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Year:  1998        PMID: 9475097      PMCID: PMC1051189          DOI: 10.1136/jmg.35.1.58

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  10 in total

1.  Misalignment of pulmonary veins and alveolar capillary dysplasia.

Authors:  C Langston
Journal:  Pediatr Pathol       Date:  1991 Jan-Feb

2.  Pulmonary hypertension of the newborn and urogenital anomalies in two male siblings: a new family with misalignment of pulmonary vessels.

Authors:  S Manouvrier-Hanu; L Devisme; I Farre; V Hue; L Storme; N Kacet; O Boute-Benejean; J P Farriaux
Journal:  Genet Couns       Date:  1996

3.  Misalignment of lung vessels: a syndrome causing persistent neonatal pulmonary hypertension.

Authors:  C A Wagenvoort
Journal:  Hum Pathol       Date:  1986-07       Impact factor: 3.466

4.  Misalignment of lung vessels and alveolar capillary dysplasia: a cause of persistent pulmonary hypertension.

Authors:  G Cater; D W Thibeault; E C Beatty; H W Kilbride; M Huntrakoon
Journal:  J Pediatr       Date:  1989-02       Impact factor: 4.406

5.  Misalignment of pulmonary veins with alveolar capillary dysplasia: affected siblings and variable phenotypic expression.

Authors:  S Boggs; M C Harris; D J Hoffman; R Goel; D McDonald-McGinn; C Langston; E Zackai; E Ruchelli
Journal:  J Pediatr       Date:  1994-01       Impact factor: 4.406

Review 6.  Persistent pulmonary hypertension in the neonate: diagnosis and management.

Authors:  W W Fox; S Duara
Journal:  J Pediatr       Date:  1983-10       Impact factor: 4.406

7.  Familial persistent pulmonary hypertension.

Authors:  I Shohet; B Reichman; G Schibi; M Brish
Journal:  Arch Dis Child       Date:  1984-08       Impact factor: 3.791

Review 8.  Persistent pulmonary hypertension of the newborn due to alveolar capillary dysplasia.

Authors:  C Cullinane; P N Cox; M M Silver
Journal:  Pediatr Pathol       Date:  1992 Jul-Aug

9.  Primary alveolar capillary dysplasia.

Authors:  B Newman; E Yunis
Journal:  Pediatr Radiol       Date:  1990

10.  Congenital alveolar capillary dysplasia: a developmental vascular anomaly causing persistent pulmonary hypertension of the newborn.

Authors:  J Khorsand; R Tennant; C Gillies; A F Phillipps
Journal:  Pediatr Pathol       Date:  1985
  10 in total
  14 in total

1.  Prolonged survival in alveolar capillary dysplasia syndrome.

Authors:  Christoph Licht; Sabine Schickendantz; Narayanswami Sreeram; Georg Arnold; Rainer Rossi; Anne Vierzig; Udo Mennicken; Bernhard Roth
Journal:  Eur J Pediatr       Date:  2003-12-16       Impact factor: 3.183

Review 2.  Alveolar capillary dysplasia.

Authors:  Naomi B Bishop; Pawel Stankiewicz; Robin H Steinhorn
Journal:  Am J Respir Crit Care Med       Date:  2011-03-11       Impact factor: 21.405

3.  16q24.1 microdeletion in a premature newborn: usefulness of array-based comparative genomic hybridization in persistent pulmonary hypertension of the newborn.

Authors:  Flore Zufferey; Danielle Martinet; Maria-Chiara Osterheld; Florence Niel-Bütschi; Eric Giannoni; Nathalie Besuchet Schmutz; Zhilian Xia; Jacques S Beckmann; Charles Shaw-Smith; Pawel Stankiewicz; Claire Langston; Florence Fellmann
Journal:  Pediatr Crit Care Med       Date:  2011-11       Impact factor: 3.624

4.  A familial case of alveolar capillary dysplasia with misalignment of pulmonary veins supports paternal imprinting of FOXF1 in human.

Authors:  Partha Sen; Romana Gerychova; Petr Janku; Marta Jezova; Iveta Valaskova; Colby Navarro; Iris Silva; Claire Langston; Stephen Welty; John Belmont; Pawel Stankiewicz
Journal:  Eur J Hum Genet       Date:  2012-09-19       Impact factor: 4.246

Review 5.  An official American Thoracic Society clinical practice guideline: classification, evaluation, and management of childhood interstitial lung disease in infancy.

Authors:  Geoffrey Kurland; Robin R Deterding; James S Hagood; Lisa R Young; Alan S Brody; Robert G Castile; Sharon Dell; Leland L Fan; Aaron Hamvas; Bettina C Hilman; Claire Langston; Lawrence M Nogee; Gregory J Redding
Journal:  Am J Respir Crit Care Med       Date:  2013-08-01       Impact factor: 21.405

6.  Misplaced pulmonary arteries in an adult patient with pulmonary hypertension.

Authors:  G B Marshall; C I S Silva; J C English; R D Levy; N L Müller
Journal:  Br J Radiol       Date:  2010-01       Impact factor: 3.039

7.  Misalignment of lung vessels: diagnostic role of conventional histology and immunohistochemistry.

Authors:  Angela Pucci; Cristina Zanini; Federica Ferrero; Riccardo Arisio; Andrea Valori; Piero Abbruzzese; Marco Forni
Journal:  Virchows Arch       Date:  2003-05-13       Impact factor: 4.064

8.  Alveolar capillary dysplasia presenting as pneumothorax: a case report and review of literature.

Authors:  Pankaj G Roy; Prerna Patel; Anitha Vayalakkad; Colene Bowker; Kokila Lakhoo
Journal:  Pediatr Surg Int       Date:  2007-09       Impact factor: 1.827

9.  Genomic and genic deletions of the FOX gene cluster on 16q24.1 and inactivating mutations of FOXF1 cause alveolar capillary dysplasia and other malformations.

Authors:  Paweł Stankiewicz; Partha Sen; Samarth S Bhatt; Mekayla Storer; Zhilian Xia; Bassem A Bejjani; Zhishuo Ou; Joanna Wiszniewska; Daniel J Driscoll; Melissa K Maisenbacher; Juan Bolivar; Mislen Bauer; Elaine H Zackai; Donna McDonald-McGinn; Małgorzata M J Nowaczyk; Mitzi Murray; Virginia Hustead; Kristin Mascotti; Regina Schultz; Lavinia Hallam; Duncan McRae; Andrew G Nicholson; Robert Newbury; Jane Durham-O'Donnell; Gail Knight; Usha Kini; Tamim H Shaikh; Vicki Martin; Matthew Tyreman; Ingrid Simonic; Lionel Willatt; Joan Paterson; Sarju Mehta; Diana Rajan; Tomas Fitzgerald; Susan Gribble; Elena Prigmore; Ankita Patel; Lisa G Shaffer; Nigel P Carter; Sau Wai Cheung; Claire Langston; Charles Shaw-Smith
Journal:  Am J Hum Genet       Date:  2009-06-04       Impact factor: 11.025

10.  Prenatal Diagnosis of Cystic Hygroma related to a Deletion of 16q24.1 with Haploinsufficiency of FOXF1 and FOXC2 Genes.

Authors:  Matthew J Garabedian; Donna Wallerstein; Nubia Medina; James Byrne; Robert J Wallerstein
Journal:  Case Rep Genet       Date:  2012-08-28
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