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202 Possible Causes for Diarrhea, Reduced Fetal Movement

  • Fetal Distress in Labor

    Gestational diabetes; Post-term pregnancy; Medically induced labor; Decreased maternal blood volume, or hypovolemia, due to blood loss or body fluid loss through vomiting and diarrhea[] Signs and symptoms of fetal distress include: Reduced fetal movement or lack of movement altogether Meconium (fetal feces) in amniotic fluid Decreased heart rate A significant[] […] delivery of the fetus and the placenta, and is often preceded by signs and symptoms such as: Lower abdomen cramps similar to those accompanying menstruation Low back ache Diarrhea[]

  • Pheochromocytoma

    Common severe (Common Terminology Criteria for Adverse Events v3.0 grades 3-5) toxicities were as follows: hypertension (3/6), (Takotsubo) cardiomyopathy (2/6), diarrhea ([] Symptomatic relief of pain, headaches, diarrhea, or sweating occurred in 6 out of 10 symptomatic pts.[] Severe headaches Excessive sweating Warmth, flushing Fast heart rate and pounding heart beat Sensation of a panic attack Blurred vision Nausea, vomiting, constipation or diarrhea[]

  • Perinatal Lethal Gaucher Disease

    However, it had an adverse effect on the GI tract, including diarrhea, nausea, and vomiting, and limited indications for Gaucher disease when a patient was unable to use ERT[] The fourth pregnancy initially appeared to be progressing normally, although the mother did comment that she felt fetal movement was somewhat reduced.[] Feeding difficulties, vomiting, diarrhea, cholestatic jaundice, and recurrent respiratory infections are also common.[]

  • Congenital Muscular Dystrophy

    During the infancy, the child suffered from unexplained diarrhea and failure to thrive.[] The pregnancy history displays reduced fetal movements and poli-hydramnios. Clinical signs are present at birth.[] Suggestive of a prenatal origin of the hypotonia in infancy are the following: family history (consanguineity, familial muscle disorder); pregnancy history (reduced fetal[]

  • Spinal Muscular Atrophy

    Three patients developed adverse events that led to withdrawal from the study; one had chronic diarrhea, and two had weight gain deemed unacceptable by the parents.[] We present a male patient with SMAX2 who presented with typical symptoms at birth, preceded by reduced fetal movements in the second and third trimesters of pregnancy.[] Here we report a male infant who presented from birth with predominantly truncal hypotonia following an antenatal history of reduced fetal movements.[]

  • Smith Lemli Opitz Syndrome

    The third patient diagnosed with SLOS at birth presented at age 7months with fever and diarrhea and was noted to have profound hyponatremia.[] The patient’s serum electrolyte abnormalities are likely due to poor feeding and the diarrhea due to bile acids deficiency.[]

  • Prader-Willi Syndrome

    At the time of its IPO, Zafgen reported that the most common side effects from beloranib were nausea, vomiting, diarrhea, and sleep trouble.[] In fetal life: Reduced fetal movements and abnormal position Polyhydramnios Requirement for caesarean section In neonates and children: Feeding difficulties (poor suckling[] Prenatal Development Most pregnancies of children with PWS are uneventful, though reduced fetal movement is noted in the majority of PWS pregnancies.[]

  • Miller Dieker Syndrome

    XLAG is characterized by congenital or postnatal microcephaly, neonatal-onset intractable epilepsy, poor temperature regulation, chronic diarrhea, and abnormal genitalia [[] History of polyhydramnios, intrauterine growth retardation and reduced fetal movements are associated with MDS.[]

  • Hyper IgD Syndrome

    Attacks were often accompanied by rash and severe stomach ache and diarrhea.[] The earliest warning of the condition in most recent series has been reduced fetal body movements accompanied by sinusoidal fetal heart rate patterns and altered fetal biophysical[] Her parents and elder brother had no history of recurrent fever, prolonged abdominal pain or diarrhea of unknown origin.[]

  • Autosomal-Recessive Non-Lethal Multiple Pterygium Syndrome

    […] type 2 with microvillus atrophy MYO5B Diarrhea type 6 GUCY2C Dyschromatosis universalis hereditaria type 3 ABCB6 Dyskeratosis congenita, autosomal dominant type 1 TERC Dyskeratosis[] From Etiology see pathology Pathology nonlethal form of arthrogryposis multiplex congenita congenital contractures may be caused by reduced fetal movements at sensitive times[] Congenital contractures are common and may be caused by reduced fetal movements at sensitive times of development.[]

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