## Abstract We report on a Japanese girl and her mother with brachydactyly. Their 2nd and 5th middle phalanges were short and the latter was fused with the distal phalanx in one of the patients. Length and shape of proximal and distal phalanges as well as metacarpals seemed normal. These findings a
Brachydactyly and short stature in a kindred with early-onset parkinsonism
โ Scribed by Dekker, Marieke C.J. ;Galjaard, R.J.H. ;Snijders, P.J.L.M. ;Heutink, P. ;Oostra, B.A. ;van Duijn, C.M.
- Publisher
- John Wiley and Sons
- Year
- 2004
- Tongue
- English
- Weight
- 122 KB
- Volume
- 130A
- Category
- Article
- ISSN
- 0148-7299
No coin nor oath required. For personal study only.
โฆ Synopsis
Abstract
In a Dutch kindred we have identified a deletion of the DJโ1 gene, leading to autosomalโrecessive parkinsonism. The parkinsonism patients also had short stature and brachydactyly. In the family and a control group from the same community, we used the DJโ1 deletion as a marker for the originally linked PARK7 region and found a significant association with body height (Pโ=โ0.005), which suggests a gene in linkage disequilibrium with DJโ1 to be implicated in short stature. Analysis of handโbone length showed incomplete segregation of the PARK7 region with brachydactyly, such that a gene in PARK7 is unlikely to fully explain the brachydactyly. Since the bone length reduction was more pronounced in the homozygous parkinsonism patients than in their heterozygous relatives, however, the PARK7 region may contain a modifier gene for growth. ยฉ 2004 WileyโLiss, Inc.
๐ SIMILAR VOLUMES
## Abstract We screened for mutations in the __PARKIN__, __DJโ1__, and __PINK1__ genes in a Taiwanese cohort (68 probands; 58 sporadic and 10 familial) with earlyโonset parkinsonism (EOP, onset <50 years of age). We identified 9 patients harboring mutations in __PARKIN__ (three compound heterozygou
We report on clinical (18)F-labeled 6-fluorodopa ((18)F-dopa) positron emission tomography (PET) and molecular genetic analyses of an ethnic Chinese family in which three siblings presented with early-onset Parkinson's disease. As described in some parkin patients, neither sleep benefit nor diurnal
## Abstract In 1989, Tsukahara and colleagues described a single female with a provisionally unique pattern of malformation consisting of low intelligence, short stature, brachydactyly type A1, and characteristic facial features. We report on a second patient confirming Tsukahara syndrome as an est