All Madelung deformities are not endocrine
- PMID: 24251169
- PMCID: PMC3830315
- DOI: 10.4103/2230-8210.119581
All Madelung deformities are not endocrine
Abstract
Madelung deformity is a rare inherited disorder associated with endocrine disorders like Turner's syndrome, pseudohypoparathyroidism, but can be seen with short stature homeobox deficiency conditions such as Leri-Weill dyschondrosteosis (LWD) and Langers mesomelic dysplasia. It has also been reported following trauma to the distal radius epiphysis neoplasia mucopolysaccharidosis (MPS) and achondroplasia. Madelung deformity is an abnormality of distal radial epiphysis where in progressive ulnar and volar tilt of the articular surface occurring in association with distal subluxation of ulna. A 13-year-old girl was referred to us for evaluation of bilateral deformity of wrist and short stature. There was ulnar deviation and dorsal tilt of bilateral hands without history of pain to the joint trauma and family history of similar illness. On X-ray, wrist showed malformed distal radial epiphysis with dorsal and ulnar shift and with increased length of phalanges suggestive of Madelung deformity. X-ray spine was normal. Ultrasound abdomen showed normal uterus and ovary and her follicle stimulating hormone. Luteinizing hormone was normal and so was urine MPS screening. Based on the above points the diagnosis of LWD was made.
Keywords: Achondroplasia; Madelung; dyschondrosteosis.
Conflict of interest statement
Figures
References
-
- Léri A, Weill JA. Une affection congénitale et symétrique dudéveloppement osseux. La dyschondrostéose. Bull Mem Soc Med Hop Paris. 1929;53:1491–4.
-
- Langer LO., Jr Dyschondrosteosis, a hereditable bone dysplasia with characteristic roentgenographic features. Am J Roentgenol Radium Ther Nucl Med. 1965;95:178–88. - PubMed
-
- Clement-Jones M, Schiller S, Rao E, Blaschke RJ, Zuniga A, Zeller R, et al. The short stature homeobox gene SHOX is involved in skeletal abnormalities in Turner syndrome. Hum Mol Genet. 2000;9:695–702. - PubMed
-
- Blaschke RJ, Rappold G. The pseudoautosomal regions, SHOX and disease. Curr Opin Genet Dev. 2006;16:233–9. - PubMed
-
- Marchini A, Rappold G, Schneider KU. SHOX at a glance: From gene to protein. Arch Physiol Biochem. 2007;113:116–23. - PubMed
Publication types
LinkOut - more resources
Full Text Sources
Other Literature Sources
Research Materials
