Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Krishna Chaithanya Battu"'
Publikováno v:
Pediatric Review: International Journal of Pediatric Research. 7:442-445
A congenital variant of rett syndrome or Forkhead box G1 (FOXG1) syndrome is a rareneurodevelopmental disorder characterized by global developmental delay, microcephaly, autisticfeatures, early-onset dyskinesia, and seizures. Once it was described as
Publikováno v:
Journal of Pediatric Epilepsy. :048-050
Idiopathic ketotic hypoglycemia (IKH) is characterized by recurrent neurohypoglycemic symptoms with ketosis. Hypoglycemic episodes typically occur during early mornings, especially either with illness and/or prolonged fasting. We reported a case of I
Publikováno v:
International Journal of Contemporary Pediatrics. 7:2077
Hereditary spastic paraplegia (HSP) is a clinically and genetically heterogeneous group of neurological disorders that are characterized by progressive spasticity of the lower extremities. It can present as pure form or complex form. It can be presen
Autor:
Sai Chandar D; Pediatric Neurology, Star Women and Children Hospital, Karim Nagar, IND.; Pediatrics, Prathima Institute of Medical Sciences, Karim Nagar, IND., Krishna Chaithanya B; Pediatrics, Star Women and Children Hospital, Karim Nagar, IND., Prashanthi M; Pediatrics, Prathima Institute of Medical Sciences, Karim Nagar, IND.
Publikováno v:
Cureus [Cureus] 2021 Apr 28; Vol. 13 (4), pp. e14727. Date of Electronic Publication: 2021 Apr 28.