When children have problems coordinating movements, they may have dyspraxia. This is a lifelong disorder in learning how to move. The causes cannot be treated; however, targeted therapy interventions can significantly improve patients’ gross and fine motor skills. What is dyspraxia? Dyspraxia is a lifelong coordination and developmental disorder also known as clumsy child syndrome. … Dyspraxia: Causes, Symptoms & Treatment
Infantile sputum (meconium) is the name given to the first stool of a newborn baby, which is greenish-black in color. Usually babies excrete it within 12 to 48 hours, but for some the excretion occurs in the womb, which can lead to a condition called meconium aspiration syndrome. What is puerperal meconium? Infantile saliva or … Kindspech
Induction of labor is the artificial triggering of birth using various hormonal substances, with the triggering occurring before the onset of labor. Artificial induction of labor is performed for a wide variety of reasons. What is induction of labor? Induction of labor is the artificial triggering of birth using various hormonal substances, with the triggering … Induction of Labor: Treatment, Effects & Risks
Intrauterine growth retardation refers to a prenatal disorder of development. Synonyms for intrauterine growth retardation are prenatal dystrophy and fetal hypertrophy. What is intrauterine growth retardation? Intrauterine growth retardation is a pathologic delay in the growth of an unborn child in the uterus (womb). Affected infants are referred to as SGA infants. SGA stands for … Intrauterine Growth Retardation: Causes, Symptoms & Treatment
Crane-Heise syndrome is the medical term for a complex of malformations consisting mainly of insufficient ossification of the skull and aplasia of the vertebrae. The syndrome is due to a hereditary mutation, which is based on an autosomal recessive inheritance. The prognosis is unfavorable and the course is usually lethal. What is Crane-Heise syndrome? Crane-Heise … Crane-Heise Syndrome: Causes, Symptoms & Treatment
Hers disease is assigned to the group of glycogen storage diseases and represents a disease that is characterized in most cases by a deficiency of a specific enzyme. This enzyme is the so-called alpha-glucan phosphorylase enzyme, which is found particularly in the liver. What is Hers disease? Hers disease is a metabolic disorder in which … Hers Disease: Causes, Symptoms & Treatment