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3,440 Possible Causes for Diabetes Insipidus, No Polydactyly, Onset of Renal Dysfunction in Early Childhood

  • Alstrom Syndrome

    A case of Alström syndrome associated with diabetes insipidus. Clin Genet. 1995;48:164-166. 17. Michaud JL, Heon E, Guilbert F, et al.[] Sufferers often develop early-onset type 2 diabetes, renal and hepatic dysfunction affecting the liver and kidneys, bladder and bowel problems, and cardiomyopathy, where the[] […] childhood, progressive neurosensory hearing loss, diabetes mellitus, acanthosis nigricans, hypogonadism with normal secondary sex characteristics, and kyphoscoliosis without polydactyly[]

  • Laurence Moon Syndrome

    Polyuria and/or polydipsia (nephrogenic diabetes insipidus) 5. Ataxia, poor coordination, imbalance 6. Mild spasticity (especially lower limbs) 7. Diabetes mellitus 8.[] Figure 2: showing polydactyly in lower limbs Figure 3: showing polydactyly in left hand Figure 4: showing high arched palate.[] Insipidus 136 TreacherCollins Syndrome 15 Growth Hormone Deficiency 137 Triploidy SyndromePartial Molar Pregnancy 16 HAIRAN Syndrome 138 Turner Syndrome 17 Hermaphroditism[]

    Missing: Onset of Renal Dysfunction in Early Childhood
  • Hypothalamic Hamartoma

    One child developed a mild postoperative right hemiparesis and one developed transient diabetes insipidus. There were no adverse developmental effects of surgery.[] […] of inherited syndromes that have in common anomalies of the tongue (bifid or lobulated tongue with hamartomas), the face (median cleft lip) and the digits (brachydactyly, polydactyly[] Diabetes insipidus is commonly encountered postoperatively, but is not observed with HH prior to surgical intervention.[]

    Missing: Onset of Renal Dysfunction in Early Childhood
  • 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.[] The case was also diagnosed as having holoprosencephaly-polydactyly syndrome (pseudotrisomy 13) because she had alobar holoprosencephaly, preaxial polydactyly, facial dysmorfism[] One of our cases had a clinical picture similar to that of holoprosencephaly-polydactyly syndrome. The other had the rare anatomical finding of a polylobuated spleen.[]

    Missing: Onset of Renal Dysfunction in Early Childhood
  • Panhypopituitarism

    To our knowledge, this is the first reported case of AF presenting as panhypopituitarism with central diabetes insipidus.[] , Royal Adelaide Hospital, North Terrace, Adelaide, South Australia. Abstract We describe a male patient with ocular colobomata, cleft palate, polydactyly[] 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[]

    Missing: Onset of Renal Dysfunction in Early Childhood
  • Hydronephrosis

    ., diabetes insipidus, psychogenic polydipsia) Hydronephrosis of infection: due to bacterial toxins inhibiting smooth muscle contraction of the renal pelvis and ureter Pediatric[] No polydactyly.[] Pseudotrisomy 13 syndrome (holoprosencephaly-polydactyly) In this case we have not sent 7-DHC level.[]

    Missing: Onset of Renal Dysfunction in Early Childhood
  • Frontonasal Dysplasia

    insipidus and pituitary dysfunction.[] This form of frontonasal dysplasia was documented previously in a few other cases with various combinations of postaxial polydactyly, tibial hypoplasia, epibulbar dermoid,[] […] superior vermis, hypoplastic cerebellum and brain stem, and possible posterior fossa cyst in this case); short neck, relatively long trunk with short limbs; cryptorchidism; and polydactyly[]

    Missing: Onset of Renal Dysfunction in Early Childhood
  • Cenani Syndactylism

    insipidus 1 ) · PTGER2 ( Aspirin-induced asthma ) Class B PTH1R ( Jansen's metaphyseal chondrodysplasia ) Class C CASR ( Familial hypocalciuric hypercalcemia ) Class F FZD4[] Novick, Car***"Polydactyly of the Foot." eMedicin*** "Polydactyly." Health Library. "Polydactyly and Syndactyly."[] ( Male-limited precocious puberty ) · FSHR ( XX gonadal dysgenesis ) · EDNRB ( ABCD syndrome , Waardenburg syndrome 4a , Hirschsprung's disease 2 ) · AVPR2 ( Nephrogenic diabetes[]

    Missing: Onset of Renal Dysfunction in Early Childhood
  • Acrocallosal Syndrome

    insipidus) in which a mirror duplication of nearly the entire short arm of chromosome 12 was discovered.[] Major characteristics of the acrocallosal syndrome include severe mental retardation, agenesis or hypoplasia of the corpus callosum, and polydactyly of fingers and toes.[] Our patient also had the Dandy-Walker malformation, imperforate anus with rectovaginal fistula, hypothalamic dysfunction with hypothyroidism and diabetes insipidus, thick,[]

    Missing: Onset of Renal Dysfunction in Early Childhood
  • Hypopituitarism

    DIAGNOSIS: Central diabetes insipidus and anterior hypopituitarism secondary to Langerhans cell histiocytosis.[] In these patients, the posterior pituitary was also ectopic, but none had polydactyly.[] These findings indicate a hypothalamic type of hypopituitarism and masked central diabetes insipidus which possibly derived from the atypical occupation of Rathke's cleft[]

    Missing: Onset of Renal Dysfunction in Early Childhood

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