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179 Possible Causes for Diarrhea, Reduced Fetal Movement

  • Infantile Restrictive Dermopathy

    , or hands (especially creases), buccal membranes, nipples, genitals, and scars, vitiligo, alopecia -Hypotension, vasodilation, shock -anorexia, N&V -cramping, abd pain, diarrhea[quizlet.com] Polyhydramnios with reduced fetal movements is followed by premature delivery at around 31 weeks gestation.[thedoctorsdoctor.com] OOM #600373 CODAS syndrome OCM #216550 Cohen Syndrome A Congenital Central Hypoventilation Syndrome A #616326 Congenital Myasthenic Syndrome OOM #270420 Congenital Sodium Diarrhea[biochemgenetics.ca]

  • Antenatal Onset Minicore Myopathy with Arthrogryposis

    […] prostaglandin metabolism Polycythemia Hyperphosphatemia Anorexia Impaired reabsorption of chloride Frontal bossing Growth hormone deficiency Abnormality of the retinal vasculature Diarrhea[mendelian.co] The antenatal form with arthrogryposis is distinguished by the presence of contractures at birth due to reduced fetal movement as well as various physical anomalies.[checkorphan.org] Added to this are gastroparesis, constipation, vomiting, and intermittent diarrhea with abdominal pain.[disorders.eyes.arizona.edu]

  • Fetal Distress in Labor

    […] 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[news-medical.net] 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[birthinjuryinfo.org] 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[thecplawyer.com]

  • 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 ([ncbi.nlm.nih.gov] Symptomatic relief of pain, headaches, diarrhea, or sweating occurred in 6 out of 10 symptomatic pts.[ncbi.nlm.nih.gov] 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[winchesterhospital.org]

  • Gaucher Disease, Collodion Type

    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[bmcmedgenet.biomedcentral.com] The fourth pregnancy initially appeared to be progressing normally, although the mother did comment that she felt fetal movement was somewhat reduced.[doi.org] […] congenital failure of autonomic control , see congenital central hypoventilation syndrome congenital familial lymphedema , see Milroy disease congenital familial protracted diarrhea[elbiruniblogspotcom.blogspot.com]

  • Autosomal Dominant Benign Spinal Muscular Atrophy

    However, it is thought that carriers of CF may be more resistant to diarrhea during typhoid fever or cholera.[wikivisually.com] There may be a history of reduced fetal movements in utero. Mortality/morbidity : median survival is 7 months - 95% die before 18 months.[patient.info] 1436 Christian, síndrome de 2621 Christian-Rosenberg, síndrome de 1808 Christianson-Fourie, síndrome de Chromophobe renal cell carcinoma Chronic actinic dermatitis Chronic diarrhea[docplayer.com.br]

  • 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.[doi.org] 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.[ncbi.nlm.nih.gov] Here we report a male infant who presented from birth with predominantly truncal hypotonia following an antenatal history of reduced fetal movements.[ncbi.nlm.nih.gov]

  • Lethal Congenital Contracture Syndrome 6

    5 2 Diamond-Blackfan Anemia 6 2 Diamond-Blackfan Anemia 7 2 Diamond-Blackfan Anemia 8 2 Diamond-Blackfan Anemia 9 2 Diaphanospondylodysostosis 2 Diaphragmatic Hernia 3 1 Diarrhea[preventiongenetics.com] Drugs, including phenytoin and alcohol, can impair fetal movements. Oligohydramnios reduces fetal movements. A septate uterus or large fibroids can do the same.[patient.info] Polyhydramnios with reduced fetal movements is followed by premature delivery at around 31 weeks gestation.[thedoctorsdoctor.com]

  • Congenital Muscular Dystrophy

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

  • Miller Dieker Syndrome

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

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