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, 2007]. They proposed a new diagnostic term, ��LUMBAR�� syndrome as a more accurate and comprehensive description of the constellation of the following features: lower body infantile hemangioma and other skin defects, urogenital anomalies and ulceration, myelopathy, bony deformities, anorectal malformations, and see more arterial anomalies, and renal anomalies. The study noted hemangiomas to be segmental with minimal growth. Extensive limb hemangiomas showed potential for regional correlation with additional extracutaneous anomalies including underlying arterial anomalies, and limb underdevelopment. In this clinical report we present a male infant with the rare phenotype of LUMBAR syndrome and review the clinical manifestations of those cases previously reported. The proband, a male infant, was born at 37 and 4/7 weeks gestation to a 25-year-old gravida 1 para 0 mother and a 25-year-old father. Prenatal history was negative for maternal illness, gestational diabetes, or exposure to teratogens. Prenatal ultrasound revealed a male infant with IUGR, a single umbilical artery, learn more and intra-abdominal calcification, which was not seen after birth on ultrasound. The infant was delivered by caesarean. Birth weight was 2,170 grams (lazabemide the left buttock to the lateral aspect of the entire left leg, dorsal aspect of foot, and lateral plantar aspect of the foot. Examination of the rest of the skin was normal. High resolution karyotype analysis revealed a normal 46, XY karyotype. Fluorescence in situ hybridization with SRY probe yielded normal results. SRY sequencing has been recommended but not yet performed. MRI of the spine documented spina bifida occulta, intradural lipoma (beginning at the S1 level extending caudally), and a tethered cord. Surgery for the tethered cord was recommended after 6 months of age. Skeletal X-ray documented hemihyperplasia of the left leg which suggests underlying arterial anomalies based on previously reported cases [Iacobas et al., 2010].