Hepatoblastoma risk factors: Difference between revisions

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* Having [[Beckwith-Wiedemann syndrome]].
* Having [[Beckwith-Wiedemann syndrome]].
* Having had a very low weight at birth.
* Having had a very low weight at birth.
{| style="border: 0px; font-size: 90%; margin: 3px; width: 1000px"
|valign=top|
|+
! style="background: #4479BA; width: 250px; color: #FFFFFF;"|'''Associated Disorder'''
! style="background: #4479BA; width: 600px; color: #FFFFFF;"|'''Clinical findings'''
|-
| style="padding: 5px 5px; background: #DCDCDC; font-weight: bold" align=center | '''Aicardi syndrome'''|| style="padding: 5px 5px; background: #F5F5F5;" |
:* Agenesis of the corpus callosum, chorioretinal lacunae, and infantile spasms, with a characteristic facies.
|-
| style="padding: 5px 5px; background: #DCDCDC; font-weight: bold" align=center | '''Beckwith-Wiedemann syndrome'''|| style="padding: 5px 5px; background: #F5F5F5;"|
:* Hemihypertrophy, hemihyperplasia.
|-
| style="padding: 5px 5px; background: #DCDCDC; font-weight: bold" align=center | '''Familial adenomatous polyposis'''|| style="padding: 5px 5px; background: #F5F5F5;"|
:*
|-
| style="padding: 5px 5px; background: #DCDCDC; font-weight: bold" align=center | '''Glycogen storage diseases I–IV '''|| style="padding: 5px 5px; background: #F5F5F5;" |
:*Symptoms vary by individual disorder.
|-
| style="padding: 5px 5px; background: #DCDCDC; font-weight: bold" align=center | '''Low-birth-weight infants'''|| style="padding: 5px 5px; background: #F5F5F5;" |
:*Preterm and small-for-gestation-age neonates.
|-
| style="padding: 5px 5px; background: #DCDCDC; font-weight: bold" align=center | '''Simpson-Golabi-Behmel syndrome'''|| style="padding: 5px 5px; background: #F5F5F5;"|
:*Macroglossia, macrosomia, renal and skeletal abnormalities, and increased risk of Wilms tumor.
|-
|style="padding: 5px 5px; background: #DCDCDC; font-weight: bold" align=center | '''Trisomy 18, other trisomies'''|| style="padding: 5px 5px; background: #F5F5F5;" |
:*Trisomy 18: Microcephaly and micrognathia, clenched fists with overlapping fingers, and failure to thrive. Most patients (>90%) die in the first month of life.
|-


==References==
==References==

Revision as of 21:16, 27 October 2015

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1];Associate Editor(s)-in-Chief: Nawal Muazam M.D.[2]

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Risk factors for hepatoblastoma including the following:

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Associated Disorder Clinical findings
Aicardi syndrome
  • Agenesis of the corpus callosum, chorioretinal lacunae, and infantile spasms, with a characteristic facies.
Beckwith-Wiedemann syndrome
  • Hemihypertrophy, hemihyperplasia.
Familial adenomatous polyposis
Glycogen storage diseases I–IV
  • Symptoms vary by individual disorder.
Low-birth-weight infants
  • Preterm and small-for-gestation-age neonates.
Simpson-Golabi-Behmel syndrome
  • Macroglossia, macrosomia, renal and skeletal abnormalities, and increased risk of Wilms tumor.
Trisomy 18, other trisomies
  • Trisomy 18: Microcephaly and micrognathia, clenched fists with overlapping fingers, and failure to thrive. Most patients (>90%) die in the first month of life.