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Items: 1 to 20 of 117

1.

A fetus with hemifacial microsomia and sirenomelia. The same mesodermal defect spectrum?

López-Valdez JA, Estrada-Juárez H, Moreno-Verduzco ER, Aguinaga-Ríos M.

Fetal Pediatr Pathol. 2013 Apr;32(2):152-7. doi: 10.3109/15513815.2012.684846. Epub 2012 May 29.

PMID:
22643051
2.

A patient with VACTERL association, amelia and hemifacial microsomia.

Aftimos S, Winship I.

Clin Dysmorphol. 1999 Apr;8(2):135-7.

PMID:
10319203
3.

Caudal dysplasia syndrome and sirenomelia: are they part of a spectrum?

Bruce JH, Romaguera RL, Rodriguez MM, González-Quintero VH, Azouz EM.

Fetal Pediatr Pathol. 2009;28(3):109-31. doi: 10.1080/15513810902772383.

PMID:
19365740
4.

[Sirenomelia as a part of VACTERL association: a study of three cases].

Charlier P, Valat AS, Boute O, Petit S, Chafiotte C, Huynh-Charlier I, Gosselin B, Devisme L.

Ann Pathol. 2008 Jun;28(3):176-81. doi: 10.1016/j.annpat.2008.06.001. Epub 2008 Jul 22. French.

PMID:
18706355
5.

Sirenomelia and VACTERL association in the offspring of a woman with diabetes.

Castori M, Silvestri E, Cappellacci S, Binni F, Sforzolini GS, Grammatico P.

Am J Med Genet A. 2010 Jul;152A(7):1803-7. doi: 10.1002/ajmg.a.33460.

PMID:
20583159
6.

Overlap between VACTERL and hemifacial microsomia illustrating a spectrum of malformations seen in axial mesodermal dysplasia complex (AMDC).

Bergmann C, Zerres K, Peschgens T, Senderek J, Hörnchen H, Rudnik-Schöneborn S.

Am J Med Genet A. 2003 Aug 30;121A(2):151-5. Review.

PMID:
12910495
7.

Caudal dysgenesis and sirenomelia-single centre experience suggests common pathogenic basis.

Thottungal AD, Charles AK, Dickinson JE, Bower C.

Am J Med Genet A. 2010 Oct;152A(10):2578-87. doi: 10.1002/ajmg.a.33599.

PMID:
20734338
8.

A fetus with sirenomelia, omphalocele, and meningomyelocele, but normal kidneys.

McCoy MC, Chescheir NC, Kuller JA, Altman GC, Flannagan LM.

Teratology. 1994 Aug;50(2):168-71.

PMID:
7801305
9.

Cebocephaly, alobar holoprosencephaly, spina bifida, and sirenomelia in a stillbirth.

Chen CP, Shih SL, Liu FF, Jan SW.

J Med Genet. 1997 Mar;34(3):252-5.

10.

[Sirenomelia and multicystic renal dysplasia. Apropos of 2 cases].

Chappard D, Lauras B, Fargier P, Knopf JF.

J Genet Hum. 1983 Dec;31 Suppl 5:403-11. French.

PMID:
6674416
11.

[Sirenomelia--prenatal diagnosis and clinical consequences of a rare abnormality].

Heyl W, Funk A, Grün M, Rath W.

Z Geburtshilfe Neonatol. 1998 May-Jun;202(3):121-6. German.

PMID:
9715528
12.

[Sirenomelia--a rare cause of an oligoanhydramnion in the second trimester--a case report].

Morfeld CA, Hofstaetter C, Adolf S, Radner H, Schild RL.

Z Geburtshilfe Neonatol. 2012 Feb;216(1):34-6. doi: 10.1055/s-0031-1298030. Epub 2012 Feb 13. German.

PMID:
22331526
13.

Caudal dysgenesis, sirenomelia, and situs inversus totalis: a primitive defect in blastogenesis.

Rougemont AL, Bouron-Dal Soglio D, Désilets V, Jovanovic M, Perreault G, Laurier Oligny L, Fournet JC.

Am J Med Genet A. 2008 Jun 1;146A(11):1470-6. doi: 10.1002/ajmg.a.32081.

PMID:
18470923
14.

Interrelationships of the hemifacial microsomia-VATER, VATER, and sirenomelia phenotypes.

Duncan PA, Shapiro LR.

Am J Med Genet. 1993 Aug 1;47(1):75-84. Review.

PMID:
8368258
15.

Sirenomelia with associated systemic anomalies: an autopsy pathologic illustration of a series of four cases.

Chikkannaiah P, Mahadevan A, Gosavi M, Kangle R, Anuradha, Shankar SK.

Pathol Res Pract. 2014 Jul;210(7):444-9. doi: 10.1016/j.prp.2014.01.017. Epub 2014 Feb 28.

PMID:
24656289
16.

Craniorachischisis totalis and sirenomelia.

Rodríguez JI, Palacios J.

Am J Med Genet. 1992 Jul 1;43(4):732-6. Review.

PMID:
1621765
17.

[Hemifacial microsomia. Description of a case with associated rare multiple visceral anomalies].

Lapetina F, Romano A, Teza F, Piantoni G.

Pediatr Med Chir. 1985 May-Jun;7(3):467-70. Italian.

PMID:
3837211
18.

Sirenomelia associated with a "vanishing twin".

Kapur RP, Mahony BS, Nyberg DA, Resta RG, Shepard TH.

Teratology. 1991 Feb;43(2):103-8.

PMID:
2014475
19.

Sirenomelia in a twelve weeks abortus.

Malinger G, Treschan O, Rosen N, Zakut H.

Early Hum Dev. 1987 Jul;15(4):217-20.

PMID:
3622350
20.

Single aberrant umbilical artery in a fetus with severe caudal defects: sirenomelia or caudal dysgenesis.

Perez-Aytes A, Montero L, Gomez J, Paya A.

Am J Med Genet. 1997 Apr 14;69(4):409-12.

PMID:
9098492

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