| CASE REPORT |
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| Year : 2020 | Volume
: 9
| Issue : 4 | Page : 160-162 |
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Co-existence of russell–silver syndrome with arnold–chiari type 1: A new syndrome or just an association
Joydeep Das1, Krishnendu Choudhury1, Shweta Kothari2, Navneet Jeevan Nayek1
1 Department of Pediatrics, Jagannath Gupta Institute of Medical Sciences, Kolkata, WB, India
2 Department of Radiology, Jagannath Gupta Institute of Medical Sciences, Kolkata, WB, India
Correspondence Address:
Joydeep Das
Flat 1F, Natural Top, 77A, Christopher Road, Kolkata - 700 046, West Bengal
India
 Source of Support: None, Conflict of Interest: None
DOI: 10.4103/jpai.jpai_20_21
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Hemihypertrophy is not uncommon in pediatrics, a triad of short stature of prenatal onset, skeletal asymmetry, and clinodactyly is characteristic of Russell–Silver syndrome. Association of posterior fossa malformation of Chiari Type 1 with whole length syringomyelia is not reported in literature. We present a case with a combined feature of both syndromes.
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