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1.
Journal of Genetic Medicine ; : 93-97, 2012.
Artigo em Inglês | WPRIM | ID: wpr-137164

RESUMO

Kniest syndrome (OMIM #156550) is a rare autosomal dominant disorder caused by a dysfunction of type II collagen, which is encoded by the COL2A1 gene (OMIM +120140) mapped to chromosome 12q13.11. Type II collagen, a molecule found mostly in the cartilage and vitreous tissues, is essential for the normal development of bones and other connective tissues. Kniest syndrome is a type II collagenopathy that presents as skeletal abnormality associated with disproportionate dwarfism, kyphoscoliosis, enlarged joints, visual loss, hearing loss, and cleft palate. This report describes a Korean patient with Kniest syndrome who was diagnosed with typical clinical features and radiologic findings. The patient presented with disproportionately short stature and kyphoscoliosis from birth. A skeletal survey revealed fused lamina in the thoracic spine, hemivertebrae, flexion deformities in multiple joints, and plagiocephaly.


Assuntos
Humanos , Cartilagem , Fissura Palatina , Colágeno Tipo II , Anormalidades Congênitas , Tecido Conjuntivo , Nanismo , Perda Auditiva , Articulações , Parto , Plagiocefalia , Coluna Vertebral
2.
Journal of Genetic Medicine ; : 93-97, 2012.
Artigo em Inglês | WPRIM | ID: wpr-137161

RESUMO

Kniest syndrome (OMIM #156550) is a rare autosomal dominant disorder caused by a dysfunction of type II collagen, which is encoded by the COL2A1 gene (OMIM +120140) mapped to chromosome 12q13.11. Type II collagen, a molecule found mostly in the cartilage and vitreous tissues, is essential for the normal development of bones and other connective tissues. Kniest syndrome is a type II collagenopathy that presents as skeletal abnormality associated with disproportionate dwarfism, kyphoscoliosis, enlarged joints, visual loss, hearing loss, and cleft palate. This report describes a Korean patient with Kniest syndrome who was diagnosed with typical clinical features and radiologic findings. The patient presented with disproportionately short stature and kyphoscoliosis from birth. A skeletal survey revealed fused lamina in the thoracic spine, hemivertebrae, flexion deformities in multiple joints, and plagiocephaly.


Assuntos
Humanos , Cartilagem , Fissura Palatina , Colágeno Tipo II , Anormalidades Congênitas , Tecido Conjuntivo , Nanismo , Perda Auditiva , Articulações , Parto , Plagiocefalia , Coluna Vertebral
3.
Korean Journal of Fertility and Sterility ; : 307-311, 1993.
Artigo em Coreano | WPRIM | ID: wpr-214709

RESUMO

No abstract available.


Assuntos
Humanos , Diabetes Mellitus , Insulina , Puberdade Tardia
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