Lethal multiple pterygium syndrome (LMPS) is an autosomal recessive disorder characterized by fetal hy pokinesia wit]h consequent j oint contractures , pterygia and intrauterine death . Retronuchal cystic hygroma and hydrops are frequent as sociated findings [De Die Smulders et al . , 1 9 90] . The pathogenesis of LMPS is still unknown . An abnormal fragile collagen constitu tion [Hartwig et al . , 1 989] and, more recently, a pri mary aplasia of the developing muscle fibers [Moerman et al . , 1 990 ] have been proposed . We report on a case of LMPS in a 22 -week-old fetus of healthy, unrelated parents with a history of fetal death in 2 of 3 former pregnancie s and one normal 6-year-old son
We report the prenatal sonographic detection of a fetus with megalencephaly, polymicrogyria, postaxi...
Popliteal pterygium syndrome (PPS) is an extremely rare autosomal dominant disorder, characterized b...
Leroy I-cell disease is a rare autosomal recessive lysosomal storage disorder characterized by marke...
Lethal multiple pterygium syndrome is a rare inherited disorder. Previous reports suggest that the d...
Lethal multiple pterygium (LMP) is a series of disorders of fetal formation with a heterogeneous ran...
Multiple pterygium sendromu (MPS) anormal yüz görünümü ve antekübital, servikal, popliteal, interdig...
AbstractFetal akinesia deformation sequence is a clinically and genetically heterogeneous disorder c...
INTRODUCTION: Foetal akinesia deformation sequence syndrome (FADS) is a genetically heterogeneous di...
[[abstract]]Fetal akinesia deformation sequence is a clinically and genetically heterogeneous disord...
Background: Multiple pterygium syndrome (MPS) is a genetically heterogeneous rare form of arthrogryp...
Copyright © 2009 Elsevier. All rights reserved.Pterygium syndrome is a complex and rare congenital d...
Multiple pterygium syndrome (MPS) is a very rare autosomal recessive disorder characterized by flexi...
In this paper we report a case of early onset fetal akinesia, with unusual pathological findings. T...
Background: At least 20 inborn errors of metabolism may cause hydrops fetalis. Most of these are lys...
BACKGROUND: At least 20 inborn errors of metabolism may cause hydrops fetalis. Most of these are lys...
We report the prenatal sonographic detection of a fetus with megalencephaly, polymicrogyria, postaxi...
Popliteal pterygium syndrome (PPS) is an extremely rare autosomal dominant disorder, characterized b...
Leroy I-cell disease is a rare autosomal recessive lysosomal storage disorder characterized by marke...
Lethal multiple pterygium syndrome is a rare inherited disorder. Previous reports suggest that the d...
Lethal multiple pterygium (LMP) is a series of disorders of fetal formation with a heterogeneous ran...
Multiple pterygium sendromu (MPS) anormal yüz görünümü ve antekübital, servikal, popliteal, interdig...
AbstractFetal akinesia deformation sequence is a clinically and genetically heterogeneous disorder c...
INTRODUCTION: Foetal akinesia deformation sequence syndrome (FADS) is a genetically heterogeneous di...
[[abstract]]Fetal akinesia deformation sequence is a clinically and genetically heterogeneous disord...
Background: Multiple pterygium syndrome (MPS) is a genetically heterogeneous rare form of arthrogryp...
Copyright © 2009 Elsevier. All rights reserved.Pterygium syndrome is a complex and rare congenital d...
Multiple pterygium syndrome (MPS) is a very rare autosomal recessive disorder characterized by flexi...
In this paper we report a case of early onset fetal akinesia, with unusual pathological findings. T...
Background: At least 20 inborn errors of metabolism may cause hydrops fetalis. Most of these are lys...
BACKGROUND: At least 20 inborn errors of metabolism may cause hydrops fetalis. Most of these are lys...
We report the prenatal sonographic detection of a fetus with megalencephaly, polymicrogyria, postaxi...
Popliteal pterygium syndrome (PPS) is an extremely rare autosomal dominant disorder, characterized b...
Leroy I-cell disease is a rare autosomal recessive lysosomal storage disorder characterized by marke...