Literature DB >> 20012803

Freeman-Sheldon syndrome--prenatal and postnatal diagnosis.

Sridevi S Hegde1, Mitesh S Shetty, B S Rama Murthy.   

Abstract

A six-day-old girl, born to normal non-consanguineous parents presented with mask like facies with a small mouth giving a 'whistling' appearance. Other dysmorphic features include deep set eyes, broad nasal bridge, long philtrum and 'H' shaped cutaneous dimple on the chin. There was congenital windmill vane hand position and severe talipes equinovarus deformity. The above features are characteristic of Freeman-Sheldon syndrome also known as Whistling Face syndrome. Ultrasound scanning during 8(th) month of the pregnancy showed the fetus to have facial abnormality and bilateral clenched hand and talipes with extension contractures of knees. Provisional diagnosis of FSS was made which was confirmed after the birth. Thus all cases of Arthrogryposis during prenatal scan should be carefully looked for the facial abnormality in the fetus.

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Year:  2009        PMID: 20012803     DOI: 10.1007/s12098-009-0227-6

Source DB:  PubMed          Journal:  Indian J Pediatr        ISSN: 0019-5456            Impact factor:   1.967


  7 in total

1.  The "whistling face" characteristic in a compound cranio-facio-corporal syndrome.

Authors:  F BURIAN
Journal:  Br J Plast Surg       Date:  1963-04

2.  Cranio-carpo-tarsal dystrophy.

Authors:  E A Freeman; J H Sheldon
Journal:  Arch Dis Child       Date:  1938-09       Impact factor: 3.791

Review 3.  A revised and extended classification of the distal arthrogryposes.

Authors:  M Bamshad; L B Jorde; J C Carey
Journal:  Am J Med Genet       Date:  1996-11-11

4.  Mutations in embryonic myosin heavy chain (MYH3) cause Freeman-Sheldon syndrome and Sheldon-Hall syndrome.

Authors:  Reha M Toydemir; Ann Rutherford; Frank G Whitby; Lynn B Jorde; John C Carey; Michael J Bamshad
Journal:  Nat Genet       Date:  2006-04-16       Impact factor: 38.330

5.  Severe form of Freeman-Sheldon syndrome associated with brain anomalies and hearing loss.

Authors:  G Zampino; G Conti; F Balducci; M Moschini; M Macchiaiolo; P Mastroiacovo
Journal:  Am J Med Genet       Date:  1996-03-29

6.  Prenatal diagnosis of Freeman-Sheldon syndrome and usefulness of an ultrasound fetal lip width normogram.

Authors:  Antonella Vimercati; Marco Scioscia; Maria Gabriella Burattini; Giovanni Pontrelli; Luigi E Selvaggi
Journal:  Prenat Diagn       Date:  2006-08       Impact factor: 3.050

7.  Clinical characteristics and natural history of Freeman-Sheldon syndrome.

Authors:  David A Stevenson; John C Carey; Janice Palumbos; Ann Rutherford; Joyce Dolcourt; Michael J Bamshad
Journal:  Pediatrics       Date:  2006-03       Impact factor: 7.124

  7 in total
  3 in total

1.  Freeman-sheldon syndrome.

Authors:  Sajad Ahmad Salati; Mahboob Hussain
Journal:  APSP J Case Rep       Date:  2013-01-01

2.  Two novel mutations in myosin binding protein C slow causing distal arthrogryposis type 2 in two large Han Chinese families may suggest important functional role of immunoglobulin domain C2.

Authors:  Xuefu Li; Bomeng Zhong; Weitian Han; Ning Zhao; Wei Liu; Yu Sui; Yawen Wang; Yongping Lu; Hong Wang; Jianxin Li; Miao Jiang
Journal:  PLoS One       Date:  2015-02-13       Impact factor: 3.240

Review 3.  Freeman-Burian syndrome.

Authors:  Mikaela I Poling; Craig R Dufresne; Robert L Chamberlain
Journal:  Orphanet J Rare Dis       Date:  2019-01-10       Impact factor: 4.123

  3 in total

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