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16 in total

1. Arachnodactyly (Marfan's syndrome) with arthrogryposis multiplex congenita.

Authors: R S DAYAL; R PRASAD; G P MATHUR
Journal: Indian J Child Health Date: 1962-09

2. Arachnodactyly associated with aneurysm of the aorta.

Authors: H S TRAISMAN; F R JOHNSON
Journal: AMA Am J Dis Child Date: 1954-02

3. "New" syndrome of congenital contractural arachnodactyly originally described by Marfan in 1896.

Authors: F Hecht; R K Beals
Journal: Pediatrics Date: 1972-04 Impact factor: 7.124

4. Cardiac manifestations of Marfan syndrome in infancy and childhood.

Authors: C Phornphutkul; A Rosenthal; A S Nadas
Journal: Circulation Date: 1973-03 Impact factor: 29.690

5. Congenital contractural arachnodactyly: a syndrome simulating Marfan's syndrome.

Authors: R B Lowry; V C Guichon
Journal: Can Med Assoc J Date: 1972-09-23 Impact factor: 8.262

6. Hereditary dysplasia of bone with kyphoscoliosis, contractures, and abnormally shaped ears.

Authors: C J Epstein; C B Graham; W E Hodgkin; F Hecht; A G Motulsky
Journal: J Pediatr Date: 1968-09 Impact factor: 4.406

7. The malformation complex of the absence of the arch of the aorta--Steidele's complex.

Authors: J T Lie
Journal: Am Heart J Date: 1967-05 Impact factor: 4.749

8. Marfan's syndrome associated with arthrogryposis in a family.

Authors: S Ghosh
Journal: Indian Pediatr Date: 1966-09 Impact factor: 1.411

Review 9. The Stickler syndrome (hereditary arthroophthalmopathy).

Authors: J Herrmann; T D France; J W Spranger; J M Opitz; C Wiffler
Journal: Birth Defects Orig Artic Ser Date: 1975

10. Marfan's syndrome (arachnodactyly) with arthrogryposis (amyoplasia congenita).

Authors: R REEVE; H K SILVER; P FERRIER
Journal: AMA J Dis Child Date: 1960-01

3 in total

1. Cardiac anomalies complicating congenital contractural arachnodactyly.

Authors: A J Macnab; L D'Orsogna; D E Cole; P E Baguley; R J Adderley; M W Patterson
Journal: Arch Dis Child Date: 1991-10 Impact factor: 3.791

2. Familial occurrence of typical and severe lethal congenital contractural arachnodactyly caused by missplicing of exon 34 of fibrillin-2.

Authors: M Wang; C L Clericuzio; M Godfrey
Journal: Am J Hum Genet Date: 1996-11 Impact factor: 11.025

3. Congenital diaphragmatic eventration and bilateral uretero-hydronephrosis in a patient with neonatal Marfan syndrome caused by a mutation in exon 25 of the FBN1 gene and review of the literature.

Authors: Nicole Revencu; Geneviève Quenum; Thierry Detaille; Gaston Verellen; Anne De Paepe; Christine Verellen-Dumoulin
Journal: Eur J Pediatr Date: 2003-10-30 Impact factor: 3.183

3 in total