Create issue ticket

963 Possible Causes for Agenesis of Corpus Callosum, Diabetes Insipidus

  • Septo-Optic Dysplasia

    An uncommon association of infantile spasms, septo-optic dysplasia, partial agenesis of the corpus callosum and an interhemispheric cyst is described in a child.[] Hypopituitarism ranges from isolated to multiple hormone deficits, with diabetes insipidus in a minority.[] In a discrete number of cases, schizencephaly, agenesis of the corpus callosum or other cortical malformations are associated (SOD-plus).[]

  • Isolated optic nerve hypoplasia

    (For more information on hypothyroidism, hypoglycemia and diabetes insipidus, please see the Related Disorders section of this report.)[] Tang PH, Bartha AI, Norton ME et al (2009) Agenesis of corpus callosum: an MR imaging analysis of associated abnormalities in the fetus.[] […] of the corpus callosum, dysplasia of the anterior third ventricle, and anomalies of the hypothalamic-pituitary axis.[]

  • Alobar Holoprosencephaly

    Abstract A 2-year-old girl with alobar holoprosencephaly associated with facial abnormalities, central diabetes insipidus, and a neuronal migration disorder is reported.[] AGENESIS OF THE CORPUS CALLOSUM Agenesis of the corpus callosum Agenesis of the corpus callosum and pachygyria.[] An infant is described with coloboma of the right eye, holoprosencephaly and diabetes insipidus without craniofacial malformations.[]

  • Hypothalamic Hamartoma

    Magnetic resonance imaging (MRI) revealed a rare combination of HH and partial agenesis of the corpus callosum (ACC).[] One child developed a mild postoperative right hemiparesis and one developed transient diabetes insipidus. There were no adverse developmental effects of surgery.[] Diabetes insipidus is commonly encountered postoperatively, but is not observed with HH prior to surgical intervention.[]

  • Basal Encephalocele

    insipidus, adipsia with essential hypernatremia and poikilothermia.[] A characteristic malformation complex consisting of median cleft face syndrome, optic nerve dysplasia, and agenesis of the corpus callosum was associated in two cases; the[] Occasional abnormalities include median cleft hp and palate, basal encephalocele, and agenesis of the corpus callosum [11].[]

  • Frontonasal Dysplasia

    insipidus and pituitary dysfunction.[] Our series also had a high frequency of patients with agenesis of the corpus callosum (12 cases), basal encephalocele (10 cases), lipoma of the corpus callosum (four cases[] […] of the corpus callosum).[]

  • Panhypopituitarism

    To our knowledge, this is the first reported case of AF presenting as panhypopituitarism with central diabetes insipidus.[] In this report, it was described the association of the molar tooth sign, absence of pituitary gland and corpus callosum agenesis on an infant with JSRD.[] Abstract Central diabetes insipidus (DI) is a rare finding in patients with acute myeloid leukemia (AML), usually occurring in patients with chromosome 3 or 7 abnormalities[]

  • Congenital Microgastria

    Verloes et al. (1995) reported a 24-week-old fetus with arhinencephaly, agenesis of the corpus callosum, hypothalamic hamartoblastoma, absence of the right thumb, hypoplastic[] We report a first case of a 4.5-year-old girl with congenital microgastria in association with growth hormone deficiency, diabetes insipidus, brachyoesophagus, hernia of the[] Torticollis, plagiocephaly, frontal bossing, paresis of ocular muscles, microphthalmos or anophthalmia, mental retardation, arrhinencephaly, fused thalami, agenesis of corpus[]

  • Langerhans-Cell Histiocytosis

    In order to document anterior pituitary dysfunction in patients with biopsy-proven Langerhans cell histiocytosis (LCH) and diabetes insipidus and to correlate this with structural[] Diabetes insipidus with impaired osmotic regulation in septo-optic dysplasia and agenesis of the corpus callosum.[] Diabetes insipidus (DI) is the most frequent central nervous system (CNS)-related permanent consequence in Langerhans cell histiocytosis (LCH), which mostly requires life-long[]

  • Empty Sella Syndrome

    […] the corpus callosum and empty sella, an interhemispheric lipoma with callosal dysgenesis, and an arachnoid cyst in the posterior fossa, respectively.[] The empty-sella syndrome should be included among the causes of arginine-vasopressin deficient diabetes insipidus in pediatric patients.[] […] of the corpus callosum (occurs in 10% of cases) musculoskeletal anomalies shortened 4 th metacarpal bones bifid rib or other rib abnormality (fusion, partial agenesis, etc[]

Further symptoms

Similar symptoms