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Медицинская библиотека · Tanisal ve girisimsel radyoloji : Tibbi Goruntuleme ve Girisimsel Radyoloji Dernegi yayin organi · 2003

[Associated brain anomalies and clinical findings in corpus callosum dysgenesis].

Alkan Alpay, Kutlu Ramazan, Baysal Tamer, Siğirci Ahmet, Altinok Tayfun, Orkan Ismet, Hallaç Tarik, Saraç Kaya

Аннотация на английскомСтатьяПеревод в очереди

Аннотация

PURPOSE: The aim of this study was to evaluate the relationship between the types of the corpus callosum dysgenesis, the associated brain anomalies and clinical findings.

MATERIALS AND

METHODS

We analyzed the MR imaging findings in 169 patients with callosal dysgenesis. Corpus callosum dysgenesis was categorized into agenesis, hypogenesis and hypoplasia. The associated brain anomalies and clinical findings were evaluated.

RESULTS

Associated brain anomalies were observed in 148 patients (87.5%). Twenty-one patients (12.4%) had isolated corpus callosum dysgenesis. Dysgenesis included agenesis in 22 (%13), hypogenesis in 46 (27.2%), and hypoplasia in 101 (59.7%) patients. The clinical findings were most commonly observed in patients with hypoplasia.

CONCLUSION

The presence of corpus callosum dysgenesis is a strong indication of possible associated brain anomalies. Corpus callosum dysgenesis and associated brain anomalies should be investigated in children with developmental delay, seizures and microcephaly.

Для цитирования: Alkan Alpay, Kutlu Ramazan, Baysal Tamer, Siğirci Ahmet, Altinok Tayfun, Orkan Ismet, Hallaç Tarik, Saraç Kaya. [Associated brain anomalies and clinical findings in corpus callosum dysgenesis].. Tanisal ve girisimsel radyoloji : Tibbi Goruntuleme ve Girisimsel Radyoloji Dernegi yayin organi. 2003.

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