Gamuts

Nephroblastomatosis

Perlman syndrome (PS) (also called renal hamartomas, nephroblastomatosis and fetal gigantism) is a rare overgrowth disorder present at birth. It is characterized by polyhydramnios and fetal overgrowth, including macrocephaly, neonatal macrosomia, visceromegaly, dysmorphic facial features, and an increased risk for Wilms' tumor at an early age. [Source: Wikipedia ]

May Cause
Bilateral large kidneys
Large kidneys with multifocal masses
Neonatal renal mass
Renal mass in a child
T2-intermediate renal mass
May Be Caused by
Aneuploidy
Aniridia-Wilms tumor association
Asplenia with liver malformation
Beckwith-Wiedemann syndrome
Bloom syndrome
Brachmann-de Lange syndrome
Chromosome 15q deletion
Congenital heart disease
Congenital obstructive uropathy-renal hamartoma-nephroblastomatosis
Epidermal nevus syndrome
Familial Wilms tumor
Frasier syndrome
Hemihypertrophy
Hereditary multiple exostoses
Horseshoe kidney
Hyperparathyroidism-jaw tumor syndrome
Klippel-Trénaunay-Weber syndrome
Li-Fraumeni syndrome
Male pseudohermaphroditism
Neurofibromatosis type 1
Perlman syndrome
Pleuropulmonary blastoma-Wilms tumor association
Poland syndrome
Prader-Willi syndrome
Premature chromatid separation
Robin sequence
Silver-Russell syndrome
Simpson-Golabi-Behmel syndrome
Trisomy 13
Trisomy 18
WAGR syndrome
Wilms tumor-hyponatremic/hypertension syndrome
Wilms tumor-multiple lung hamartomas

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