Literature DB >> 7891381

Two fetuses with Fryns syndrome without diaphragmatic defects.

K K Wilgenbus1, R Engers, G Crombach, F Majewski.   

Abstract

We report two fetuses with Fryns syndrome including the typical facial appearance and distal limb and lung hypoplasia, but no diaphragmatic hernias. The parents were consanguineous. Characteristic in both cases were the distal limb defects with brachytelephalangism and aplasia of the distal phalanges of the first toe. Since one of the two sibs had severe lung hypoplasia without macroscopic or microscopic defects of the diaphragm, we show that lung hypoplasia can occur independently from diaphragmatic defects in Fryns syndrome.

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Year:  1994        PMID: 7891381      PMCID: PMC1016700          DOI: 10.1136/jmg.31.12.962

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


  12 in total

1.  Fryns syndrome: an autosomal recessive disorder associated with craniofacial anomalies, diaphragmatic hernia, and distal digital hypoplasia.

Authors:  C Cunniff; K L Jones; H M Saal; H J Stern
Journal:  Pediatrics       Date:  1990-04       Impact factor: 7.124

2.  Terminal deletion of 6q and Fryns syndrome: a microdeletion/syndrome pair?

Authors:  N Krassikoff; G S Sekhon
Journal:  Am J Med Genet       Date:  1990-07

3.  A new lethal syndrome with cloudy corneae, diaphragmatic defects and distal limb deformities.

Authors:  J P Fryns; F Moerman; P Goddeeris; C Bossuyt; H Van den Berghe
Journal:  Hum Genet       Date:  1979       Impact factor: 4.132

4.  Fryns syndrome.

Authors:  R F Stratton; R S Young; H S Heiman; J M Carter
Journal:  Am J Med Genet       Date:  1993-03-01

5.  Fryns syndrome: a new variable multiple congenital anomaly (MCA) syndrome.

Authors:  M Lubinsky; C Severn; J M Rapoport
Journal:  Am J Med Genet       Date:  1983-03

6.  Fryns syndrome in a girl born to consanguineous parents.

Authors:  U Schwyzer; J Briner; A Schinzel
Journal:  Acta Paediatr Scand       Date:  1987-01

7.  The syndrome of diaphragmatic hernia, abnormal face and distal limb anomalies (Fryns syndrome): report of two sibs with further delineation of this multiple congenital anomaly (MCA) syndrome.

Authors:  P Moerman; J P Fryns; K Vandenberghe; H Devlieger; J M Lauweryns
Journal:  Am J Med Genet       Date:  1988-12

8.  Ring chromosome 15 in a patient with features of Fryns' syndrome.

Authors:  G de Jong; R A Rossouw; A E Retief
Journal:  J Med Genet       Date:  1989-07       Impact factor: 6.318

Review 9.  Fryns syndrome: report on 8 new cases.

Authors:  S Aymé; C Julian; D Gambarelli; B Mariotti; A Luciani; N Sudan; N Maurin; N Philip; F Serville; D Carles
Journal:  Clin Genet       Date:  1989-03       Impact factor: 4.438

10.  The Fryns syndrome: diaphragmatic defects, craniofacial dysmorphism, and distal digital hypoplasia. Further evidence for autosomal recessive inheritance.

Authors:  P Meinecke; J P Fryns
Journal:  Clin Genet       Date:  1985-12       Impact factor: 4.438

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  1 in total

Review 1.  Genetic aspects of human congenital diaphragmatic hernia.

Authors:  B R Pober
Journal:  Clin Genet       Date:  2008-05-28       Impact factor: 4.438

  1 in total

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