Medicine:Perlman syndrome
| Perlman syndrome | |
|---|---|
| Other names | Nephroblastomatosis-fetal ascites-macrosomia-Wilms tumor syndrome |
| Specialty | Medical genetics, pediatric oncology |
| Symptoms | Overgrowth, kidney dysplasia, facial dysmorphisms |
| Complications | Wilms' tumor |
| Usual onset | Prenatal or at birth |
| Duration | Lifelong |
| Causes | DIS3L2 mutation |
| Differential diagnosis | Beckwith–Wiedemann syndrome, Simpson–Golabi–Behmel syndrome |
| Prognosis | High neonatal mortality |
| Frequency | 30 reported cases[1] |
Perlman syndrome (PS), also known as nephroblastomatosis-fetal ascites-macrosomia-Wilms tumor syndrome, is a rare overgrowth syndrome caused by autosomal recessive mutations in the DIS3L2 gene. PS is characterized by macrocephaly, neonatal macrosomia, nephromegaly, renal dysplasia, dysmorphic facial features, and increased risk for Wilms' tumor. The syndrome is associated with high neonatal mortality.[1][2]
Signs and symptoms
Perlman syndrome may be detected as early as gestational week 18 by prenatal ultrasound. In the first trimester, cystic hygroma and thickened nuchal translucency may be observed. Macrosomia, macrocephaly, enlarged kidneys, macroglossia, cardiac abnormalities, and visceromegaly may become evident by the second and third trimesters.[1][3] Polyhydramnios is frequently observed.[2]
Characteristic facial features of Perlman syndrome include a hypotonic appearance with an open mouth, macrocephaly, upsweeping anterior scalp line, deep-set eyes, depressed nasal bridge, everted upper lip, and mild micrognathia.[4]
Diagnosis is made based on the individual's phenotypic features and confirmed by histologic examination of the kidneys and/or molecular genetic testing.[2] Bilateral kidney hamartomas with or without nephroblastomatosis are commonly observed.[4][5]
Genetics
Perlman syndrome is caused by mutations in the DIS3L2 gene found on chromosome 2 at 2q37.2. DIS3L2 is involved in RNA degradation and cell cycle control.[6] PS is genetically distinct from Beckwith–Wiedemann syndrome and Simpson–Golabi–Behmel syndrome, which are caused by mutations in 11p15.5 and GPC3 respectively.[1] It is inherited in an autosomal recessive manner.[7]
Management and prognosis
Perlman syndrome is associated with a high neonatal death rate due to renal failure and/or refractory hypoxemia.[8] Most individuals who survive beyond the neonatal period develop a Wilms' tumor; nearly all display some degree of developmental delay.[2][9] Treatment is supportive in nature.[1]
Epidemiology
Perlman syndrome is a rare disease with an estimated incidence of less than 1 in 1,000,000. As of 2008, fewer than 30 patients had ever been reported in the world literature.[1] PS has been described in both consanguineous and non-consanguineous couplings. The observed sex ratio is 2 males : 1 female.[10]
See also
- Beckwith–Wiedemann syndrome
- Simpson–Golabi–Behmel syndrome
- Multiple abnormalities
- Overgrowth syndrome
- Wilms' tumor
References
- ↑ 1.0 1.1 1.2 1.3 1.4 1.5 "Perlman syndrome". Orphanet. May 2008. http://www.orpha.net//consor/cgi-bin/OC_Exp.php?Lng=GB&Expert=2849.
- ↑ 2.0 2.1 2.2 2.3 Alessandri JL, Cuillier F, Ramful D, Ernould S, Robin S, de Napoli-Cocci S (2008). "Perlman syndrome: report, prenatal findings and review". Am J Med Genet A 146A (19): 2532–7. doi:10.1002/ajmg.a.32391. PMID 18780370.
- ↑ Benacerraf, Beryl R. (2007), Ultrasound of fetal syndromes (2 ed.), Elsevier Health Sciences, p. 147, ISBN 978-0-443-06641-2, https://books.google.com/books?id=1MHFF0UOKAUC
- ↑ 4.0 4.1 Perlman M (December 1986). "Perlman syndrome: familial renal dysplasia with Wilms tumor, fetal gigantism, and multiple congenital anomalies.". Am J Med Genet 25 (Pt 4): 793–5. doi:10.1002/ajmg.1320250418. PMID 3024486.
- ↑ Liban E, Kozenitzky IL (1970). "Metanephric hamartomas and nephroblastomatosis in siblings.". Cancer 25 (4): 885–8. doi:10.1002/1097-0142(197504)35:4<1212::AID-CNCR2820350427>3.0.CO;2-2. PMID 4315293.
- ↑ Astuti D, Morris MR, Cooper WN, Staals RH, Wake NC, Fews GA (2012). "Germline mutations in DIS3L2 cause the Perlman syndrome of overgrowth and Wilms tumor susceptibility.". Nat Genet 44 (3): 277–84. doi:10.1038/ng.1071. PMID 22306653.
- ↑ Neri G, Martini-Neri ME, Katz BE, Opitz JM (1984). "The Perlman syndrome: familial renal dysplasia with Wilms tumor, fetal gigantism and multiple congenital anomalies.". Am J Med Genet 19 (1): 195–207. doi:10.1002/ajmg.1320190120. PMID 6093533.
- ↑ Rimoin DL, Emery AEH (2007). Emery and Rimoin's Principles and Practice of Medical Genetics. 2 (5 ed.). Churchill Livingstone Elsevier. p. 1522. ISBN 978-0-443-06870-6. https://books.google.com/books?id=FfxPAQAAIAAJ.
- ↑ Piccione M, Cecconi M, Giuffrè M, Lo Curto M, Malacarne M, Piro E (2005). "Perlman syndrome: clinical report and nine-year follow-up.". Am J Med Genet A 139A (2): 131–5. doi:10.1002/ajmg.a.30994. PMID 16278893.
- ↑ Piccione, Maria; Corsello, Giovanni (2006-12-01). "Perlman syndrome (renal hamartomas, nephroblastomatosis and fetal gigantism)". Institute for Biomedical Research of Salamanca. https://atlasgeneticsoncology.org/cancer-prone-disease/10117/perlman-syndrome-(renal-hamartomas-nephroblastomatosis-and-fetal-gigantism).
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