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    Date Issued1990 - 2000 (1)1988 - 1989 (1)Author
    Townes, Phillip L. (2)
    Balaji, Kethandapatti C. (1)Hopkins, Timothy B. (1)Magee, B. Dale (1)Patil, Ashwinikumar (1)View MoreUMass Chan AffiliationDepartment of Pediatrics (2)Department of Obstetrics and Gynecology (1)Department of Radiology (1)Document TypeJournal Article (2)Keyword*Diseases in Twins; Humans; Infant, Newborn; Male; Polymorphism, Restriction Fragment Length; *Prune Belly Syndrome; *Twins, Monozygotic (1)Adult (1)Anencephaly (1)atelencephaly (1)autosomal recessive (1)View MoreJournalAmerican journal of medical genetics (1)Urology (1)

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    Concordant prune belly syndrome in monozygotic twins

    Balaji, Kethandapatti C.; Patil, Ashwinikumar; Townes, Phillip L.; Primack, William A.; Skare, James; Hopkins, Timothy B. (2000-06-01)
    We report 2 cases of concordant prune belly syndrome occurring in monozygotic twins. In addition to suggesting a genetic basis for this disease, our 12-year follow-up of these cases illustrates that these patients with an otherwise poor prognosis can have normal growth, development, and renal function with appropriate treatment.
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    XK aprosencephaly and anencephaly in sibs

    Townes, Phillip L.; Reuter, Karen L.; Rosquete, E. E.; Magee, B. Dale (1988-03-01)
    Recent studies have suggested a causal and pathogenetic relationship between holoprosencephaly and anencephaly. In support of the proposed relationship we report a sibship that includes anencephalic male twins and a female infant with a severe form of alobar holoprosencephaly, radial aplasia, and oligodactyly. The upper limb and brain malformations are considered to represent aprosencephaly syndrome. The coexistence of anencephaly and aprosencephaly within a sibship suggests that XK aprosencephaly syndrome may be an autosomal recessive disorder.
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