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93 Possible Causes for Blood in Stool, Occipital Encephalocele

  • Meckel-Gruber Syndrome

    A one-day-old girl was admitted to our clinic with occipital encephalocele, polydactyly, ulnar deviation of left hand and failure to thrive.[] It typically involves occipital encephalocele, polycystic kidneys, and postaxial polydactyly. Various additional abnormalities may occur simultaneously.[] Meckel-Gruber syndrome (MGS) is a rare autosomal recessive disorder which is characterized by a classic triad of occipital encephalocele, polycystic kidneys and postaxial[]

  • Cystic Kidney

    He reported no recent dysuria, diarrhea, hematuria, hematochezia, or melena.[] encephalocele Polydactyly Craniofacial dysplasia Small to normal-sized kidneys Polydipsia and polyuria Mild proteinuria with benign urinary sediment ESRD possibly during[] […] or blood in the stool Weight loss Seizures Confusion, decreased alertness, coma Exams and Tests The health care provider will examine you and ask about your symptoms.[]

  • Renal Pelvic Calculus

    Test of the stool for occult blood is negative. Administration of which of the following drugs is most likely to improve this patient's mental status. A. Bisacodyl B.[] In addition to polycystic kidney disease, this lethal syndrome includes occipital encephalocele, polydactyly, and severe oligohydramnios.[]

  • Endometrial Polyp

    Spigelian hernia Peritoneal Peritonitis ( Spontaneous bacterial peritonitis ) - Hemoperitoneum - Pneumoperitoneum نزيف معدي معوي Upper ( Hematemesis, Melena ) - Lower ( Hematochezia[] Images of the fetal brain related to Dandy-Walker malformation, Aneurysm of Vein of Galen, Acrania, Choroid plexus cyst, and Occipital meningocele with encephalocele.[]

  • Congenital Hepatic Fibrosis

    He had anuria of 3-h evolution with high risk for multiple organ failure as well as hematochezia.[] Meckel syndrome (MKS) is a perinatal lethal disorder characterized by renal cystic dysplasia, CHF, postaxial polydactyly, and occipital encephalocele or other central nervous[] Cystic fibrosis (CF) In newborns, lack of stool in the first 24-48 hours after birth (meconium ileus) Chronic diarrhea or bulky, foul-smelling, greasy stools; Blood in stool[]

  • Congenital Liver Cirrhosis

    He had anuria of 3-h evolution with high risk for multiple organ failure as well as hematochezia.[] encephalocele, and polydactyly.[] These include: Lab tests (blood, urine, and stool). Liver enzyme tests. Special blood tests to check if the liver is red or swollen (inflamed). Liver function tests.[]

  • Meningioma

    All of these events were grade 1, and included hematochezia (n 1), microscopic hematuria (n 3) and bleeding into a meningioma along the vermis (grade 1; n 1).[] We present a case of an adult woman with CSF rhinorrhea following resection of an occipital meningioma.[] The cribriform plate defect containing the encephalocele was diagnosed by computed tomography and magnetic resonance imaging.[]

  • Hirschsprung's Disease

    HAEC and inflammatory bowel disease (IBD) have similar clinical presentation including diarrhea, hematochezia, and abdominal pain.[] ., occipital encephalocele and tracheo-esophageal fistula). Possible reasons for such phenotypic variability are briefly discussed.[] This can be serious, so call your doctor right away if your child has the following symptoms: vomiting fever swollen stomach abnormal fatigue blood in the stool.[]

  • Goldenhar Syndrome

    Findings from the routine investigations of blood, urine, stool, eye swab, intelligence test and electrocardiogram were normal.[] encephalocele, agenesis of corpus callosum, hypoplasia of septum pellucidum). [ 7 ] There may also be facial nerve palsy.[] encephalocele), and anomalies of the larynx and lungs (tracheoesophageal fistula, esophageal atresia). • Complex retardation of mental development. • Venous anomalies- like[]

  • X-linked Distal Spinal Muscular Atrophy Type 3

    A complete blood count and blood, urine, and cerebrospinal fluid cultures were all within normal limits. A culture of her stool was positive for Clostridium botulinum.[] Barisic et al (2015) stated that Meckel-Gruber syndrome is a rare autosomal recessive lethal ciliopathy characterized by the triad of cystic renal dysplasia, occipital encephalocele[]

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