Literature DB >> 26178231

Bilateral patellar tendon-bearing Symes-type prostheses in a severe case of Freeman-Sheldon syndrome in a 21-year-old woman presenting with uncorrectable equinovarus.

Rodger J McCormick1, Mikaela I Poling1, Robert L Chamberlain1.   

Abstract

Described is the use of bilateral patellar tendon-bearing Symes-type prostheses in a severe case of Freeman-Sheldon syndrome (FSS) in a 21-year-old woman presenting with uncorrectable equinovarus and multiple surgical sequela of the lower extremities. FSS is considered a type of myopathic distal arthrogryposis; diagnosis requires the following: microstomia, whistling-face appearance, H-shaped chin dimpling, nasolabial folds, and multiple contractures of the hands and feet. Spinal deformities, metabolic and gastroenterological problems, other dysmorphic craniofacial characteristics, and visual and auditory impairments, are frequent findings. We highlight what we believe to be a unique approach to enhancing the patient's ability to ambulate and engage in physical activity, particularly critical determinates of wellness and long-term functional outcome in FSS, when the feet are non-correctable but not amputated. Important implications exist for physiatrists, other rehabilitation providers and surgeons regarding this likely under-diagnosed syndrome. 2015 BMJ Publishing Group Ltd.

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Year:  2015        PMID: 26178231      PMCID: PMC4513510          DOI: 10.1136/bcr-2015-211338

Source DB:  PubMed          Journal:  BMJ Case Rep        ISSN: 1757-790X


  5 in total

1.  Cranio-carpo-tarsal dystrophy.

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

2.  Genotype-phenotype relationships in Freeman-Sheldon syndrome.

Authors:  Anita E Beck; Margaret J McMillin; Heidi I S Gildersleeve; Kathryn M B Shively; Andy Tang; Michael J Bamshad
Journal:  Am J Med Genet A       Date:  2014-09-25       Impact factor: 2.802

3.  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

4.  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

5.  [Dislocation of patella also a symptom of other diseases or consequence of local primary alteration of the scelet (author's transl)].

Authors:  A Rütt
Journal:  Z Orthop Ihre Grenzgeb       Date:  1976-06
  5 in total
  3 in total

Review 1.  Identification and Recent Approaches for Evaluation and Management of Rehabilitation Concerns for Patients with Freeman-Burian Syndrome: Principles for Global Treatment.

Authors:  Mikaela I Poling; Craig R Dufresne; Rodger J McCormick
Journal:  J Pediatr Genet       Date:  2020-05-07

2.  Freeman-Sheldon syndrome in a 29-year-old woman presenting with rare and previously undescribed features.

Authors:  Robert L Chamberlain; Mikaela I Poling; Augusto L Portillo; Andrés Morales; Rigoberto R T Ramirez; Rodger J McCormick
Journal:  BMJ Case Rep       Date:  2015-10-22

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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