Pediatric and Neonatal Genetics

Pediatric and neonatal genetics provides comprehensive care within the diagnosis, treatment and prevention of birth defects, structural abnormalities, inherited diseases, chromosomal abnormalities and retardation . Pediatric and neonatal geneticists treat genetic diseases, analyze chromosomes, perform amniocentesis for diagnostic technique , conduct molecular and DNA diagnostics, and provide guidance a number of the Conditions evaluated Pediatric Geneticists include autism, birth defects and congenital anomalies, cardiac genetics, craniofacial genetics (irregularity of the face and skull), cystinosis (excess amounts of the aminoalkanoic acid cystine within the cells, affecting kidneys and eyes), mongolism , ehlers-danlos, autosomal dominant disease and marfan syndromes (disorders of animal tissue , including skin and joints), fragile x syndrome (inherited mental impairment), neurofibromatosis (nervous system disorder which can affect skin and bone), skeletal abnormalities and limb defects, urogenital malformation (defects in urogenital apparatus or genitalia), among others.

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