Literature DB >> 7243441

The axial mesodermal dysplasia spectrum.

L J Russell, D D Weaver, M J Bull.   

Abstract

Features of both the Goldenhar and the caudal regression syndromes were found in the patient described. A search of the literature revealed two other patients having both conditions. However, a number of other individuals have been reported with Goldenhar or related syndromes who have malformations in the caudal region or, conversely, who have the caudal regression syndrome and possess cranial anomalies. Possible explanations for the commonality of malformations seen in these syndromes are presented and discussed. It is suggested that the term, "axial mesodermal dysplasia spectrum" be used in patients manifesting this overlap to emphasize the importance of searching for the other malformations seen in this spectrum of anomalies.

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Year:  1981        PMID: 7243441

Source DB:  PubMed          Journal:  Pediatrics        ISSN: 0031-4005            Impact factor:   7.124


  22 in total

1.  Cebocephaly, alobar holoprosencephaly, spina bifida, and sirenomelia in a stillbirth.

Authors:  C P Chen; S L Shih; F F Liu; S W Jan
Journal:  J Med Genet       Date:  1997-03       Impact factor: 6.318

2.  De novo inv(2)(p12q34) associated with Klippel-Feil anomaly and hypodontia.

Authors:  Manolis J Papagrigorakis; Philippos N Synodinos; Constandinos P Daliouris; Caterina Metaxotou
Journal:  Eur J Pediatr       Date:  2003-06-24       Impact factor: 3.183

3.  Audiological abnormalities in the Klippel-Feil syndrome.

Authors:  J M McGaughran; P Kuna; V Das
Journal:  Arch Dis Child       Date:  1998-10       Impact factor: 3.791

Review 4.  Is urorectal septum malformation sequence a variant of the vertebral defects, anal atresia, tracheo-oesophageal fistula, renal defects and radial dysplasia association? Report of a case and a review of the literature.

Authors:  Jen-Chung Chien; Shu-Jen Chen; Chui-Mei Tiu; Yann-Jang Chen; Betau Hwang; Dau-Ming Niu
Journal:  Eur J Pediatr       Date:  2005-02-24       Impact factor: 3.183

Review 5.  Oculoauriculovertebral spectrum and cerebral anomalies.

Authors:  C T Schrander-Stumpel; C E de Die-Smulders; R C Hennekam; J P Fryns; P X Bouckaert; O F Brouwer; J J da Costa; E J Lommen; P D Maaswinkel-Mooy
Journal:  J Med Genet       Date:  1992-05       Impact factor: 6.318

6.  Pierre Robin syndrome with caudal regression syndrome-a rare combination of congenital syndromes.

Authors:  Mohd Ilyas; Iqbal Bashir; Inayat Ellahi; Feroze Shaheen; Naseer Choh
Journal:  Childs Nerv Syst       Date:  2018-04-12       Impact factor: 1.475

7.  Chiari I malformation, caudal regression syndrome, and Pierre Robin Syndrome: a previously unreported combination.

Authors:  R Shane Tubbs; W Jerry Oakes
Journal:  Childs Nerv Syst       Date:  2006-10-05       Impact factor: 1.475

8.  'Inside-out', back-to-front: a model for clinical population genetic screening.

Authors:  D Shickle; I Harvey
Journal:  J Med Genet       Date:  1993-07       Impact factor: 6.318

9.  Oesophageal atresia and associated anomalies.

Authors:  S Chittmittrapap; L Spitz; E M Kiely; R J Brereton
Journal:  Arch Dis Child       Date:  1989-03       Impact factor: 3.791

Review 10.  The exstrophy-epispadias complex.

Authors:  Anne-Karoline Ebert; Heiko Reutter; Michael Ludwig; Wolfgang H Rösch
Journal:  Orphanet J Rare Dis       Date:  2009-10-30       Impact factor: 4.123

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