The Experts below are selected from a list of 1470 Experts worldwide ranked by ideXlab platform
Anne Vral - One of the best experts on this subject based on the ideXlab platform.
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seckel syndrome associated with oligodontia microdontia enamel hypoplasia delayed eruption and dentin dysmineralization a new variant
Journal of Oral Pathology & Medicine, 2006Co-Authors: P J De Coster, V Holthaus, R M H Verbeeck, Luc Martens, Anne VralAbstract:Seckel syndrome (SCKL) [OMIM Entry 210600] is a rare, autosomal recessive syndrome, characterized by severe intrauterine and postnatal growth retardation, microcephaly, mental retardation, and typical facial appearance with beaklike protrusion of the midface (bird-headed). Associated findings may include limb anomalies, dislocation of femoral heads, scoliosis, and Gastrointestinal Malformation. A 14-year-old boy is presented with brain hypoplasia, pachygyria, hydrocephaly, enamel hypoplasia and root dysplasia in the temporary dentition, and oligodontia, severe microdontia, and delayed eruption of the permanent dentition. The association of SCKL with the above unusual dental findings may represent a new phenotype.
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seckel syndrome associated with oligodontia microdontia enamel hypoplasia delayed eruption and dentin dysmineralization a new variant
Journal of Oral Pathology & Medicine, 2006Co-Authors: P J De Coster, V Holthaus, R M H Verbeeck, Luc Martens, Anne VralAbstract:Seckel syndrome (SCKL) [OMIM Entry 210600] is a rare, autosomal recessive syndrome, characterized by severe intrauterine and postnatal growth retardation, microcephaly, mental retardation, and typical facial appearance with beaklike protrusion of the midface (bird-headed). Associated findings may include limb anomalies, dislocation of femoral heads, scoliosis, and Gastrointestinal Malformation. A 14-year-old boy is presented with brain hypoplasia, pachygyria, hydrocephaly, enamel hypoplasia and root dysplasia in the temporary dentition, and oligodontia, severe microdontia, and delayed eruption of the permanent dentition. The association of SCKL with the above unusual dental findings may represent a new phenotype.
P J De Coster - One of the best experts on this subject based on the ideXlab platform.
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seckel syndrome associated with oligodontia microdontia enamel hypoplasia delayed eruption and dentin dysmineralization a new variant
Journal of Oral Pathology & Medicine, 2006Co-Authors: P J De Coster, V Holthaus, R M H Verbeeck, Luc Martens, Anne VralAbstract:Seckel syndrome (SCKL) [OMIM Entry 210600] is a rare, autosomal recessive syndrome, characterized by severe intrauterine and postnatal growth retardation, microcephaly, mental retardation, and typical facial appearance with beaklike protrusion of the midface (bird-headed). Associated findings may include limb anomalies, dislocation of femoral heads, scoliosis, and Gastrointestinal Malformation. A 14-year-old boy is presented with brain hypoplasia, pachygyria, hydrocephaly, enamel hypoplasia and root dysplasia in the temporary dentition, and oligodontia, severe microdontia, and delayed eruption of the permanent dentition. The association of SCKL with the above unusual dental findings may represent a new phenotype.
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seckel syndrome associated with oligodontia microdontia enamel hypoplasia delayed eruption and dentin dysmineralization a new variant
Journal of Oral Pathology & Medicine, 2006Co-Authors: P J De Coster, V Holthaus, R M H Verbeeck, Luc Martens, Anne VralAbstract:Seckel syndrome (SCKL) [OMIM Entry 210600] is a rare, autosomal recessive syndrome, characterized by severe intrauterine and postnatal growth retardation, microcephaly, mental retardation, and typical facial appearance with beaklike protrusion of the midface (bird-headed). Associated findings may include limb anomalies, dislocation of femoral heads, scoliosis, and Gastrointestinal Malformation. A 14-year-old boy is presented with brain hypoplasia, pachygyria, hydrocephaly, enamel hypoplasia and root dysplasia in the temporary dentition, and oligodontia, severe microdontia, and delayed eruption of the permanent dentition. The association of SCKL with the above unusual dental findings may represent a new phenotype.
V Holthaus - One of the best experts on this subject based on the ideXlab platform.
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seckel syndrome associated with oligodontia microdontia enamel hypoplasia delayed eruption and dentin dysmineralization a new variant
Journal of Oral Pathology & Medicine, 2006Co-Authors: P J De Coster, V Holthaus, R M H Verbeeck, Luc Martens, Anne VralAbstract:Seckel syndrome (SCKL) [OMIM Entry 210600] is a rare, autosomal recessive syndrome, characterized by severe intrauterine and postnatal growth retardation, microcephaly, mental retardation, and typical facial appearance with beaklike protrusion of the midface (bird-headed). Associated findings may include limb anomalies, dislocation of femoral heads, scoliosis, and Gastrointestinal Malformation. A 14-year-old boy is presented with brain hypoplasia, pachygyria, hydrocephaly, enamel hypoplasia and root dysplasia in the temporary dentition, and oligodontia, severe microdontia, and delayed eruption of the permanent dentition. The association of SCKL with the above unusual dental findings may represent a new phenotype.
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seckel syndrome associated with oligodontia microdontia enamel hypoplasia delayed eruption and dentin dysmineralization a new variant
Journal of Oral Pathology & Medicine, 2006Co-Authors: P J De Coster, V Holthaus, R M H Verbeeck, Luc Martens, Anne VralAbstract:Seckel syndrome (SCKL) [OMIM Entry 210600] is a rare, autosomal recessive syndrome, characterized by severe intrauterine and postnatal growth retardation, microcephaly, mental retardation, and typical facial appearance with beaklike protrusion of the midface (bird-headed). Associated findings may include limb anomalies, dislocation of femoral heads, scoliosis, and Gastrointestinal Malformation. A 14-year-old boy is presented with brain hypoplasia, pachygyria, hydrocephaly, enamel hypoplasia and root dysplasia in the temporary dentition, and oligodontia, severe microdontia, and delayed eruption of the permanent dentition. The association of SCKL with the above unusual dental findings may represent a new phenotype.
R M H Verbeeck - One of the best experts on this subject based on the ideXlab platform.
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seckel syndrome associated with oligodontia microdontia enamel hypoplasia delayed eruption and dentin dysmineralization a new variant
Journal of Oral Pathology & Medicine, 2006Co-Authors: P J De Coster, V Holthaus, R M H Verbeeck, Luc Martens, Anne VralAbstract:Seckel syndrome (SCKL) [OMIM Entry 210600] is a rare, autosomal recessive syndrome, characterized by severe intrauterine and postnatal growth retardation, microcephaly, mental retardation, and typical facial appearance with beaklike protrusion of the midface (bird-headed). Associated findings may include limb anomalies, dislocation of femoral heads, scoliosis, and Gastrointestinal Malformation. A 14-year-old boy is presented with brain hypoplasia, pachygyria, hydrocephaly, enamel hypoplasia and root dysplasia in the temporary dentition, and oligodontia, severe microdontia, and delayed eruption of the permanent dentition. The association of SCKL with the above unusual dental findings may represent a new phenotype.
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seckel syndrome associated with oligodontia microdontia enamel hypoplasia delayed eruption and dentin dysmineralization a new variant
Journal of Oral Pathology & Medicine, 2006Co-Authors: P J De Coster, V Holthaus, R M H Verbeeck, Luc Martens, Anne VralAbstract:Seckel syndrome (SCKL) [OMIM Entry 210600] is a rare, autosomal recessive syndrome, characterized by severe intrauterine and postnatal growth retardation, microcephaly, mental retardation, and typical facial appearance with beaklike protrusion of the midface (bird-headed). Associated findings may include limb anomalies, dislocation of femoral heads, scoliosis, and Gastrointestinal Malformation. A 14-year-old boy is presented with brain hypoplasia, pachygyria, hydrocephaly, enamel hypoplasia and root dysplasia in the temporary dentition, and oligodontia, severe microdontia, and delayed eruption of the permanent dentition. The association of SCKL with the above unusual dental findings may represent a new phenotype.
Luc Martens - One of the best experts on this subject based on the ideXlab platform.
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seckel syndrome associated with oligodontia microdontia enamel hypoplasia delayed eruption and dentin dysmineralization a new variant
Journal of Oral Pathology & Medicine, 2006Co-Authors: P J De Coster, V Holthaus, R M H Verbeeck, Luc Martens, Anne VralAbstract:Seckel syndrome (SCKL) [OMIM Entry 210600] is a rare, autosomal recessive syndrome, characterized by severe intrauterine and postnatal growth retardation, microcephaly, mental retardation, and typical facial appearance with beaklike protrusion of the midface (bird-headed). Associated findings may include limb anomalies, dislocation of femoral heads, scoliosis, and Gastrointestinal Malformation. A 14-year-old boy is presented with brain hypoplasia, pachygyria, hydrocephaly, enamel hypoplasia and root dysplasia in the temporary dentition, and oligodontia, severe microdontia, and delayed eruption of the permanent dentition. The association of SCKL with the above unusual dental findings may represent a new phenotype.
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seckel syndrome associated with oligodontia microdontia enamel hypoplasia delayed eruption and dentin dysmineralization a new variant
Journal of Oral Pathology & Medicine, 2006Co-Authors: P J De Coster, V Holthaus, R M H Verbeeck, Luc Martens, Anne VralAbstract:Seckel syndrome (SCKL) [OMIM Entry 210600] is a rare, autosomal recessive syndrome, characterized by severe intrauterine and postnatal growth retardation, microcephaly, mental retardation, and typical facial appearance with beaklike protrusion of the midface (bird-headed). Associated findings may include limb anomalies, dislocation of femoral heads, scoliosis, and Gastrointestinal Malformation. A 14-year-old boy is presented with brain hypoplasia, pachygyria, hydrocephaly, enamel hypoplasia and root dysplasia in the temporary dentition, and oligodontia, severe microdontia, and delayed eruption of the permanent dentition. The association of SCKL with the above unusual dental findings may represent a new phenotype.
