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779.32 Bilious vomiting in newborn; 779.33 Other vomiting in newborn; 779.34 Failure to thrive in newborn; 779.4 Drug reactions and intoxications specific to newborn; 779.5 Drug withdrawal syndrome in newborn; 779.6 Termination of pregnancy (fetus) 779.7 Preventricular leukomalacia; 779.8 Other specified conditions originating in the perinatal ...
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Neonatal encephalopathy (NE), previously known as neonatal hypoxic-ischemic encephalopathy (neonatal HIE or NHIE), is defined as a encephalopathy syndrome with signs and symptoms of abnormal neurological function, in the first few days of life in an infant born after 35 weeks of gestation.
An extension to ICD-9 was published in 1979. [1] [2] An extension to ICD-10 has also been published. [3] It is the basis for the U.S. Centers for Disease Control and Prevention's six digit codes for reportable congenital conditions. [4] These are also known as the "CDC/BPA codes". [5] [6] This system is in turn is the basis for the Texas ...
ICD-10 is the 10th revision of the International Classification of Diseases (ICD), a medical classification list by the World Health Organization (WHO). It contains codes for diseases, signs and symptoms, abnormal findings, complaints, social circumstances, and external causes of injury or diseases. [1]
Neonatal alloimmune thrombocytopenia (NAITP, NAIT, NATP or NAT) is a disease that affects babies in which the platelet count is decreased because the mother's immune system attacks her fetus' or newborn's platelets. A low platelet count increases the risk of bleeding in the fetus and newborn.
Newborn infant with Rhesus disease, a type of hemolytic disease of the newborn, suffering from hydrops fetalis. The infant did not survive. [4] Hydrops fetalis usually stems from fetal anemia, when the heart needs to pump a much greater volume of blood to deliver the same amount of oxygen. This anemia can have either an immune or non-immune cause.
Vitamin K deficiency bleeding (VKDB) of the newborn, previously known as haemorrhagic disease of the newborn, [1] is a rare form of bleeding disorder that affects newborns and young infants due to low stores of vitamin K at birth. [2] It commonly presents with intracranial haemorrhage with the risk of brain damage or death. [3]