Rehabilitation Treatment of a Child Diagnosed With Duplication of 1q42-q44: A Case Report
Annals of Rehabilitation Medicine
;
: 938-942, 2016.
Article
in English
| WPRIM
| ID: wpr-59042
ABSTRACT
Trisomy 1 is a rare chromosomal anomaly and has never been reported in Korea. Clinical features of trisomy 1 include macrocephaly, prominent forehead, flat nasal bridge, low set ears, and micrognathia, all of which result in a very distinguishable facial structure. A child with trisomy 1 also suffers from mental retardation and/or developmental delays. In this case report, the child was diagnosed with de novo trisomy 1 without receiving any treatment until visiting our hospital. The child suffered from foot and ankle deformities, leading her unable to stand independently. Here we report the surgical treatment and rehabilitation treatment that enabled the child to walk independently.
Full text:
Available
Index:
WPRIM (Western Pacific)
Main subject:
Rehabilitation
/
Congenital Abnormalities
/
Trisomy
/
Orthopedic Procedures
/
Ear
/
Megalencephaly
/
Foot
/
Forehead
/
Korea
/
Ankle
Type of study:
Diagnostic study
Limits:
Child
/
Humans
Country/Region as subject:
Asia
Language:
English
Journal:
Annals of Rehabilitation Medicine
Year:
2016
Type:
Article
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