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DOI 10.1177/0883073817712589

Медицинская библиотека · Journal of child neurology · 2017

The Most Common Comorbidities in Dandy-Walker Syndrome Patients: A Systematic Review of Case Reports.

Stambolliu Emelina, Ioakeim-Ioannidou Myrsini, Kontokostas Kimonas, Dakoutrou Maria, Kousoulis Antonis A

СтатьяСистематический обзорПеревод в очереди

Аннотация

OBJECTIVE

Dandy-Walker syndrome (DWS) is a rare neurologic multi-entity malformation. This review aimed at reporting its main nonneurologic comorbidities.

METHODS

Following PRISMA guidelines, search in Medline was conducted (2000-2014, keyword: dandy-walker). Age, sex, country, DWS type, consanguinity or siblings with DWS, and recorded coexistent conditions (by ICD10 category) were extracted for 187 patients (46.5% male, 43% from Asia) from 168 case reports.

RESULTS

Diagnosis was most often set in <1 year old (40.6%) or >12 years old (27.8%). One-third of cases had a chromosomal abnormality or syndrome (n = 8 PHACE), 27% had a cardiovascular condition (n = 7 Patent Ductus Arteriosus), 24% had a disease of eye and ear (n = 9 cataract); most common malignancy was nephroblastoma (n = 8, all Asian). Almost one-fifth had a mental illness diagnosis; only 6.4% had mild or severe intellectual disability.

CONCLUSION

The spread of comorbidities calls for early diagnosis and multidisciplinary research and practice, especially as many cases remain clinically asymptomatic for years.

Для цитирования: Stambolliu Emelina, Ioakeim-Ioannidou Myrsini, Kontokostas Kimonas, Dakoutrou Maria, Kousoulis Antonis A. The Most Common Comorbidities in Dandy-Walker Syndrome Patients: A Systematic Review of Case Reports.. Journal of child neurology. 2017. DOI: 10.1177/0883073817712589.

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