Klinefelter syndrome is a chromosomal disorder with a typical karyotype of 47, XXY, accompanied by various neurological symptoms. We herein report the first case of Klinefelter syndrome with a rare mosaic form of 47, XXY and 48, XXXY, combined with both spastic paraplegia and peripheral motor neuropathy. This case showed spasticity and hyperreflexia with pathological reflexes and ankle clonus as well as muscle weakness in all extremities. A motor nerve conduction study and the magnetic motor evoked potential suggested motor axonal neuropathy and corticospinal tract disorders. The present case suggests that Klinefelter syndrome can present with both upper and lower motor neuron degeneration
Angelman syndrome (AS, OMIM 105830) is a neurogenetic disorder with firm clinical diagnostic guideli...
Marker chromosomes are very rare in Klinefelter patients and phenotypic findings are related to the ...
Hereditary spastic paraplegias (HSP) are a rare heterogeneous group of inherited neurodegenerative d...
Paralysis periodica paramyotonica is an overlapping disease that shares the features of paramyotonia...
Paralysis periodica paramyotonica is an overlapping disease that shares the features of paramyotonia...
Ankylosing spondylitis is a chronic inflammatory disease characterized by inflammatory lower back pa...
Klinefelter syndrome is a disorder of variation of sex chromosome, the most common karyotype being 4...
WOS: 000382992500008PubMed ID: 2748946848,XXYY syndrome is a rare sex chromosome abnormality. Althou...
A 60-year-old male was admitted to our hospital because of orthopnea. He had been mentally retarded...
Klinefelter syndrome (KS) is the most common sex chromosomal disorder in men. Most of these patients...
A 10-year old boy presented small testicles, a small penis, hypospadia, scanty hair growth, and long...
Copyright © 2014 Javier Sánchez et al. This is an open access article distributed under the Creativ...
International audienceOsteopathia striata with cranial sclerosis is a rare X-linked disorder. It is ...
Klinefelter syndrome, the first described chromosomal abnormality, is characterized with hypergonado...
Klinefelter's syndrome is the most common genetic disorder in which there is at least one extra X ch...
Angelman syndrome (AS, OMIM 105830) is a neurogenetic disorder with firm clinical diagnostic guideli...
Marker chromosomes are very rare in Klinefelter patients and phenotypic findings are related to the ...
Hereditary spastic paraplegias (HSP) are a rare heterogeneous group of inherited neurodegenerative d...
Paralysis periodica paramyotonica is an overlapping disease that shares the features of paramyotonia...
Paralysis periodica paramyotonica is an overlapping disease that shares the features of paramyotonia...
Ankylosing spondylitis is a chronic inflammatory disease characterized by inflammatory lower back pa...
Klinefelter syndrome is a disorder of variation of sex chromosome, the most common karyotype being 4...
WOS: 000382992500008PubMed ID: 2748946848,XXYY syndrome is a rare sex chromosome abnormality. Althou...
A 60-year-old male was admitted to our hospital because of orthopnea. He had been mentally retarded...
Klinefelter syndrome (KS) is the most common sex chromosomal disorder in men. Most of these patients...
A 10-year old boy presented small testicles, a small penis, hypospadia, scanty hair growth, and long...
Copyright © 2014 Javier Sánchez et al. This is an open access article distributed under the Creativ...
International audienceOsteopathia striata with cranial sclerosis is a rare X-linked disorder. It is ...
Klinefelter syndrome, the first described chromosomal abnormality, is characterized with hypergonado...
Klinefelter's syndrome is the most common genetic disorder in which there is at least one extra X ch...
Angelman syndrome (AS, OMIM 105830) is a neurogenetic disorder with firm clinical diagnostic guideli...
Marker chromosomes are very rare in Klinefelter patients and phenotypic findings are related to the ...
Hereditary spastic paraplegias (HSP) are a rare heterogeneous group of inherited neurodegenerative d...