Medicine:Fitzsimmons–Guilbert syndrome
| Fitzsimmons–Guilbert syndrome | |
|---|---|
| Other names | Paraplegia-brachydactyly-cone-shaped epiphysis syndrome |
Fitzsimmons–Guilbert syndrome is an extremely rare genetic disease characterized by a slowly progressive spastic paraplegia, skeletal anomalies of the hands and feet with brachydactyly type E, cone-shaped epiphyses, abnormal metaphyseal–phalangeal pattern profile, sternal anomaly (pectus carinatum or excavatum), dysarthria, and mild intellectual deficit.[1]
Pathophysiology
With so few described cases, establishing the basic pathophysiological mechanisms or genetic abnormalities has not been possible.[citation needed]
Diagnosis
Treatment
History
Fitzsimmons and Guilbert first described male uniovular twins, aged 20 years, who had had slowly progressive spastic paraplegia from early in life.[2] Both had skeletal abnormalities of the hands and feet: brachydactyly, cone-shaped epiphyses, and an abnormal metaphyseal-phalangeal pattern profile. In addition, they had nonspecific dysarthria and low-normal intellectual capacity.[2]
Since the original report, three more cases have been described, including two (Lacassie et al.) with a more severe mental retardation and a different metacarpal-phalangeal pattern profile, though these cases may represent a new disease entity.[3][4]
References
- ↑ "Paraplegia – brachydactyly – cone-shaped epiphysis". ORPHANET. http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=GB&Expert=2823. Retrieved 2007-03-17.
- ↑ 2.0 2.1 "Spastic paraplegia associated with brachydactyly and cone shaped epiphyses". J Med Genet 24 (11): 702–5. 1987. doi:10.1136/jmg.24.11.702. PMID 3430547.
- ↑ Hennekam R (1994). "Spastic paraplegia, dysarthria, brachydactyly, and cone shaped epiphyses: confirmation of the Fitzsimmons syndrome". J Med Genet 31 (3): 251–2. doi:10.1136/jmg.31.3.251. PMID 8014978.
- ↑ "Identical twins with mental retardation, dysarthria, progressive spastic paraplegia, and brachydactyly type E: a new syndrome or variant of Fitzsimmons-Guilbert syndrome?". Am J Med Genet 84 (2): 90–3. 1999. doi:10.1002/(SICI)1096-8628(19990521)84:2<90::AID-AJMG2>3.0.CO;2-8. PMID 10323731.
External links
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