Literature DB >> 14653486

Torticollis in an infant caused by hereditary muscle aplasia.

Samuel B Adams1, John M Flynn, Harish S Hosalkar, Jill Hunter, Richard Finkel, Harish Halsikar.   

Abstract

Torticollis is a common condition presenting to the general or pediatric orthopedist. We describe the case of a child with severe torticollis caused by a hereditary unilateral absence of the sternocleidomastoid and trapezius muscles. Both his father and paternal grandfather had a forme fruste, with similar but milder findings. Electromyography and cross-sectional imaging were valuable in making the diagnosis. We believe this is the first reported case of hereditary unilateral muscle aplasia presenting as torticollis in an infant.

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Year:  2003        PMID: 14653486

Source DB:  PubMed          Journal:  Am J Orthop (Belle Mead NJ)        ISSN: 1078-4519


  3 in total

1.  Congenital torticollis due to sternomastoid aplasia with unilateral cerebellar hypoplasia: a rare association.

Authors:  V R Ravi Kumar; S Raja Sabapathy; Vijayagiri Duraisami
Journal:  Indian J Pediatr       Date:  2011-10-14       Impact factor: 1.967

2.  Congenital torticollis caused by unilateral absence of the sternocleidomastoid muscle.

Authors:  Subha Raman; Deepak Takhtani; E Christine Wallace
Journal:  Pediatr Radiol       Date:  2008-10-07

Review 3.  Symptomatic asymmetry in the first six months of life: differential diagnosis.

Authors:  Jacqueline Nuysink; Ingrid C van Haastert; Tim Takken; Paul J M Helders
Journal:  Eur J Pediatr       Date:  2008-03-04       Impact factor: 3.183

  3 in total

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