Freeman-Sheldon Syndrome – A Case of Rare Observation
نویسندگان
چکیده
منابع مشابه
[Freeman-Sheldon syndrome. Report of a case].
Freeman-Sheldon syndrome is a morphologically well-defined syndrome that results in a dysmorphic status combining bone anomalies and joint contractures with characteristic facies. FSS (FreemanSheldon Syndrome) is also known as craniocarpotarsal dysplasia (or dystrophy), distal arthrogryposis type IIA (DAIIA), whistling face syndrome, and whistling face-windmill vane hand syndrome. The syndrome ...
متن کاملFreeman-Sheldon syndrome: a case report.
BACKGROUND Freeman-Sheldon syndrome is a rare hereditary disorder characterised by three basic abnormalities, namely microstomia, camptodactyly with ulnar deviation of the fingers, and clubfoot. The majority of these patients have microstomia and dental crowding, making oral hygiene difficult and increasing the risk of caries. Treatment of these patients requires a coordinated effort by a team ...
متن کاملFreeman-Sheldon Syndrome
Freeman-Sheldon syndrome (FSS) is a rare inherited form of distal arthrogryposis characterized by craniofacial deformities, camptodactyly with ulnar deviation of the fingers, and talipes equinovarus. Less than hundred cases have been reported till 2010 [1-3]. Multiple surgical interventions are needed to provide an acceptable quality of life. Anesthetic complications occur commonly [4, 5]. We p...
متن کاملFreeman-Sheldon syndrome: a disorder of congenital myopathic origin?
Freeman-Sheldon syndrome was diagnosed in an unrelated adult man and woman, with severe abnormalities of the extremities but only slight anomalies of the face. Electromyography and muscle biopsy showed a myopathy which was classified as a congenital disproportion of fibre type and seemed to be the primary cause of the deformities. This allowed classification of the syndrome as a separate type o...
متن کاملFreeman-Sheldon syndrome: a functional and cosmetic correction of microstomia.
Freeman-Sheldon syndrome (FSS) is a rare form of multiple congenital contracture syndrome and is the most severe form of distal arthrogryposis. Described in 1938 by Freeman and Sheldon, it is also referred to as distal arthrogryposis type 2A, craniocarpotarsal dysplasia or whistling faceewindmill vane hand syndrome. Its main form of inheritance is autosomal dominant, but it can also be autosoma...
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ژورنال
عنوان ژورنال: Journal of Pediatrics and Mother Care
سال: 2017
ISSN: 2472-3835
DOI: 10.19104/japm.2016.110