Case Reports
doi: 10.1016/s0165-5876(03)00133-2.
Craniometaphyseal dysplasia: a case report and review of medical and surgical management
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- PMID: 12745166
- DOI: 10.1016/s0165-5876(03)00133-2
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Case Reports
Craniometaphyseal dysplasia: a case report and review of medical and surgical management
Int J Pediatr Otorhinolaryngol.
2003 Jun.
Abstract
Craniometaphyseal dysplasia (CMD) is a genetic syndrome involving cranial and tubular bone anomalies that commonly present at a young age, often with otolaryngologic manifestations. In this paper, we report a rare case of a sporadic form of the disease resulting in an early state of hypocalcemia with secondary hyperparathyroidism. A conductive hearing loss is also documented prior to 12 months of age. The clinical aspects of CMD will be covered along with its pathogenesis. The current concepts surrounding medical and surgical treatments will be reviewed, and the management of our patient will be discussed.
Corrected and republished from
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Craniometaphyseal dysplasia: a case report and review of medical and surgical management.Int J Pediatr Otorhinolaryngol. 2003 Jan;67(1):71-7. doi: 10.1016/s0165-5876(02)00289-6. Int J Pediatr Otorhinolaryngol. 2003. Corrected and republished in: Int J Pediatr Otorhinolaryngol. 2003 Jun;67(6):687-93. doi: 10.1016/s0165-5876(03)00133-2. PMID: 12560153 Corrected and republished. Review.
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Craniometaphyseal dysplasia: a case report and review of medical and surgical management.Int J Pediatr Otorhinolaryngol. 2003 Jan;67(1):71-7. doi: 10.1016/s0165-5876(02)00289-6. Int J Pediatr Otorhinolaryngol. 2003. Corrected and republished in: Int J Pediatr Otorhinolaryngol. 2003 Jun;67(6):687-93. doi: 10.1016/s0165-5876(03)00133-2. PMID: 12560153 Corrected and republished. Review.
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