Buscar
Mostrando ítems 1-10 de 25
Frontonasal dysplasia, neuronal migration error and lymphoedema of limbs
(Lippincott Williams & WilkinsPhiladelphiaEUA, 2004)
Frontonasal dysplasia, Poland anomaly and unilateral hypoplasia of lower limb: report on a male patient
(Lippincott Williams & WilkinsPhiladelphiaEUA, 2003)
Midline facial defects with hypertelorism and low-grade astrocytoma: A previously undescribed association
(Alliance Communications Group Division Allen PressLawrenceEUA, 2006)
Frontonasal dysplasia, callosal agenesis, basal encephalocele, and eye anomalies syndrome with a partial 21q22.3 deletion
(WILEY-BLACKWELLHOBOKEN, 2012)
We describe a girl with a phenotype characterized by frontonasal dysplasia, callosal agenesis, basal encephalocele, and eye anomalies who presents a 46,XX,r(21) karyotype. Array-comparative genomic hybridization using the ...
Surgical Strategies For Soft Tissue Management In Hypertelorbitism
(Lippincott Williams & WilkinsPhiladelphia, 2017)
Central nervous system abnormalities on midline facial defects with hypertelorism detected by magnetic resonance image and computed tomography
(Assoc Arquivos De Neuro- PsiquiatriaSao Paulo SpBrasil, 2006)
Cerebellar involvement in midline facial defects with ocular hypertelorism
(Alliance Communications Group Division Allen PressLawrenceEUA, 2006)
Angular analysis of corpus callosum in 18 patients with frontonasal dysplasiaAnálise angular do corpo caloso em 18 pacientes com displasia frontonasal
(Academia Brasileira de Neurologia - ABNEURO, 2004)
Pai syndrome: Report of seven South American patients
(2007)
Frontonasal dysplasia is etiologically heterogeneous and various subsets are known. Pai syndrome is one subset, which is characterized by mild hypertelorism, midline cleft lip, nasal and facial polyps, pericallosal lipoma, ...