Three cases of Japanese acromicric/geleophysic dysplasia with FBN1 mutations: a comparison of clinical and radiological features.
Kosei HasegawaChikahiko NumakuraHiroyuki TanakaMahoko FurujoToshihide KuboYousuke HiguchiMiho YamashitaHirokazu TsukaharaPublished in: Journal of pediatric endocrinology & metabolism : JPEM (2017)
Acromicric dysplasia (AD) and geleophysic dysplasia (GD) are rare skeletal dysplasias characterized by short stature, acromelia, joint contracture, hepatomegaly, hoarseness and respiratory distress. Compared with GD, AD presents with milder clinical and radiological features. Radiological findings of AD and GD consist of shortened tubular bones of the hands and feet, and deformed capital femoral epiphyses. The genetic cause of AD and some cases of GD was shown to be mutations in the transforming growth factor (TGF) β-binding protein-like domain 5 of the fibrillin 1 gene (FBN1), which is also mutated in Marfan syndrome. In the present study, we report and compare the highly varied clinical and radiological features of three Japanese AD/GD children. Our patients, harboring FBN1 mutations p.Tyr1699Cys, p.Ser1750Arg, and p.Gly1762Ser, shared common clinical symptoms such as severe short stature, acromelia and hepatomegaly. Short tubular bones of hands and deformities of femur heads are common radiological features of our patients.
Keyphrases
- transforming growth factor
- end stage renal disease
- ejection fraction
- chronic kidney disease
- binding protein
- newly diagnosed
- epithelial mesenchymal transition
- peritoneal dialysis
- prognostic factors
- gene expression
- genome wide
- physical activity
- depressive symptoms
- dna methylation
- growth hormone
- body composition
- respiratory tract