Osteopetrosis with Arnold Chiari malformation type I.
Alamelu AlagappanAmit Kumar SatpathyBiswajit SahooManoj Kumar NayakPublished in: BMJ case reports (2023)
Osteopetrosis is a rare genetic disorder resulting in increased bone density and decreased bone remodelling. Bone expansion results in the crowding of neural foramina causing cranial nerve compression. Here, we describe a female infant in her mid infancy presented with no eye contact since birth, and abdominal distension for 2 months. On CT evaluation, sclerotic bones with bilateral optic canal narrowing were present. A crowded posterior fossa with Arnold Chiari type I malformation was seen on MRI evaluation, suggesting a rare association of osteopetrosis with Arnold Chiari's malformation.
Keyphrases
- bone mineral density
- contrast enhanced
- bone loss
- soft tissue
- magnetic resonance imaging
- bone regeneration
- computed tomography
- postmenopausal women
- genome wide
- optical coherence tomography
- weight gain
- gene expression
- body mass index
- magnetic resonance
- case report
- dual energy
- positron emission tomography
- copy number
- gestational age
- pregnancy outcomes
- peripheral nerve