Total: 1 |
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PMID (PMCID) | ||
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16949239 |
MALE | |
Caudal regression syndrome associated with the white matter lesions and chromosome 18p11.2 deletion. | ||
Kacinski M, Jaworek M, Skowronek-Bala B. Brain Dev. 2007;29(3):164-6. |
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Herein, we report an unusual case of CRS associated with unspecific white matter lesions and 18p-syndrome manifested by congenital ptosis, hypothyroidism, facial dysmorphy and chromosome 18p11.2 deletion. |