Skip navigation

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Results 1 - 10 of 37 for Neonatal seizure
  1. Benign familial neonatal seizures 
    Benign familial neonatal seizures (BFNS) is a condition characterized by recurrent seizures in newborn babies. The seizures begin around day 3 of life and usually ...
    https://medlineplus.gov/.../benign-familial-neonatal-seizures - Genetics
  2. 5q31.3 microdeletion syndrome 
    ... history of the disorder in their family. Severe neonatal hypotonia-seizures-encephalopathy syndrome due to 5q31.3 microdeletion Genetic Testing Registry: PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome National Organization for Rare Disorders (NORD) ...
    https://medlineplus.gov/.../condition/5q313-microdeletion-syndrome - Genetics
  3. PURA syndrome 
    ... family. PURA-related neurodevelopmental disorder PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome Genetic Testing Registry: PURA-related severe ...
    https://medlineplus.gov/genetics/condition/pura-syndrome - Genetics
  4. Gyrate atrophy of the choroid and retina 
    ... hyperammonemia), which may lead to poor feeding, vomiting, seizures, or coma. Neonatal hyperammonemia associated with gyrate atrophy generally responds quickly ...
    https://medlineplus.gov/.../gyrate-atrophy-of-the-choroid-and-retina - Genetics
  5. HSD10 disease 
    ... the neonatal type. Males with the infantile or neonatal type frequently have weak muscle tone (hypotonia), recurrent seizures (epilepsy), and vision loss that gradually gets worse. ...
    https://medlineplus.gov/genetics/condition/hsd10-disease - Genetics
  6. Permanent neonatal diabetes mellitus 
    ... to thrive).In some cases, people with permanent neonatal diabetes mellitus also have certain neurological problems, including developmental delay and recurrent seizures (epilepsy). This combination of developmental delay, epilepsy, and ...
    https://medlineplus.gov/.../permanent-neonatal-diabetes-mellitus - Genetics
  7. MECP2-related severe neonatal encephalopathy 
    ... MECP2 gene do not develop MECP2-related severe neonatal encephalopathy. Instead, they typically develop Rett syndrome, which has signs and symptoms that include intellectual disability, seizures, and movement problems.In some cases, males with ...
    https://medlineplus.gov/...p2-related-severe-neonatal-encephalopathy - Genetics
  8. Pyridoxal phosphate-responsive seizures 
    ... symptoms of the condition. PNPO deficiency PNPO-related neonatal epileptic encephalopathy PNPOD Pyridoxal 5′-phosphate-dependent epilepsy Pyridoxal phosphate-dependent seizures Pyridoxamine 5'-oxidase deficiency Pyridoxamine 5'-phosphate oxidase ...
    https://medlineplus.gov/.../pyridoxal-phosphate-responsive-seizures - Genetics
  9. Alexander disease 
    ... of Alexander disease include speech abnormalities, swallowing difficulties, seizures, and poor coordination (ataxia). Rarely, a neonatal form of Alexander disease occurs within the first ...
    https://medlineplus.gov/genetics/condition/alexander-disease - Genetics
  10. Carnitine palmitoyltransferase II deficiency 
    ... for long periods of time, they can experience seizures or coma. Because of these serious health complications, infants with the lethal neonatal form of CPT II deficiency usually live for ...
    https://medlineplus.gov/...nitine-palmitoyltransferase-ii-deficiency - Genetics
previous · 1 · 2 · 3 · 4 · next