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Schinzel-Giedion syndrome.
Touge H, Fujinaga T, Okuda M, Aoshi H. Touge H, et al. Int J Urol. 2001 May;8(5):237-41. doi: 10.1046/j.1442-2042.2001.00291.x. Int J Urol. 2001. PMID: 11328425 Free article. Review.
Abdominal ultrasonography, computed tomography and drip infusion pyelogram showed left severe hydronephrosis and right moderate hydronephrosis. Having diagnosed Schinzel-Giedion syndrome, a left ureteroneocystostomy with tailoring was performed to preserve re …
Abdominal ultrasonography, computed tomography and drip infusion pyelogram showed left severe hydronephrosis and right moderate hydronephros …
Schinzel-Giedion syndrome: a novel case, review and revised diagnostic criteria.
Liu WL, He ZX, Li F, Ai R, Ma HW. Liu WL, et al. J Genet. 2018 Mar;97(1):35-46. J Genet. 2018. PMID: 29666323 Free article. Review.
Schinzel-Giedion syndrome (SGS) is a rare autosomal dominant inheritance disorder. ...
Schinzel-Giedion syndrome (SGS) is a rare autosomal dominant inheritance disorder. ...
Schinzel-Giedion syndrome.
Verloes A, Moës D, Palumbo L, Elmer C, François A, Bricteux G. Verloes A, et al. Eur J Pediatr. 1993 May;152(5):421-3. doi: 10.1007/BF01955902. Eur J Pediatr. 1993. PMID: 8319710
We describe a female infant with the Schinzel-Giedion syndrome. Features present in 11 patients include coarse face, midface retraction, urogenital anomalies, poor skull vault mineralisation and variable anomalies of the long bones. ...
We describe a female infant with the Schinzel-Giedion syndrome. Features present in 11 patients include coarse face, mi …
West syndrome in a patient with Schinzel-Giedion syndrome.
Miyake F, Kuroda Y, Naruto T, Ohashi I, Takano K, Kurosawa K. Miyake F, et al. J Child Neurol. 2015 Jun;30(7):932-6. doi: 10.1177/0883073814541468. Epub 2014 Jul 14. J Child Neurol. 2015. PMID: 25028416
The causative gene of Schinzel-Giedion syndrome, SETBP1, has been identified, but limited cases have been confirmed by molecular analysis. We present a 9-month-old girl affected by West syndrome with Schinzel-Giedion syndrome. Congenital …
The causative gene of Schinzel-Giedion syndrome, SETBP1, has been identified, but limited cases have been confirmed by …
Schinzel-Giedion syndrome in two Brazilian patients: Report of a novel mutation in SETBP1 and literature review of the clinical features.
Carvalho E, Honjo R, Magalhães M, Yamamoto G, Rocha K, Naslavsky M, Zatz M, Passos-Bueno MR, Kim C, Bertola D. Carvalho E, et al. Am J Med Genet A. 2015 May;167A(5):1039-46. doi: 10.1002/ajmg.a.36789. Epub 2015 Feb 7. Am J Med Genet A. 2015. PMID: 25663181
Schinzel-Giedion syndrome is a rare autosomal dominant disorder comprising postnatal growth failure, profound developmental delay, seizures, facial dysmorphisms, genitourinary, skeletal, neurological, and cardiac defects. It was recently revealed that Schi …
Schinzel-Giedion syndrome is a rare autosomal dominant disorder comprising postnatal growth failure, profound developme …
The Schinzel-Giedion syndrome. A case report and review of the literature.
Pul M, Yilmaz N, Komsuoglu B. Pul M, et al. Clin Pediatr (Phila). 1990 Apr;29(4):235-9. doi: 10.1177/000992289002900407. Clin Pediatr (Phila). 1990. PMID: 2184969 Review.
The authors discuss a 1-day-old boy who had Schinzel-Giedion syndrome. This is the fifth case reported in the literature, and it presents additional abnormalities that have not been reported previously. The Schinzel-Giedion syndrome inclu …
The authors discuss a 1-day-old boy who had Schinzel-Giedion syndrome. This is the fifth case reported in the literatur …
Hydronephrosis in Schinzel-Giedion syndrome: an important clue for the diagnosis.
Albano LM, Sakae PP, Mataloun MM, Leone CR, Bertola DR, Kim CA. Albano LM, et al. Rev Hosp Clin Fac Med Sao Paulo. 2004 Apr;59(2):89-92. doi: 10.1590/s0041-87812004000200008. Epub 2004 Apr 26. Rev Hosp Clin Fac Med Sao Paulo. 2004. PMID: 15122424
Schinzel-Giedion syndrome is a rare autosomal recessive disorder characterized by coarse facies, midface retraction, hypertrichosis, multiple skeletal anomalies, and cardiac and renal malformations. ...Of the 35 cases already reported in the literature, 31 pr …
Schinzel-Giedion syndrome is a rare autosomal recessive disorder characterized by coarse facies, midface retraction, hy …
A patient with Schinzel-Giedion syndrome and a review of 20 patients.
Okamoto N, Takeuchi M, Kitajima H, Hosokawa S. Okamoto N, et al. Jpn J Hum Genet. 1995 Jun;40(2):189-93. doi: 10.1007/BF01883576. Jpn J Hum Genet. 1995. PMID: 7662999 Review.
The Schinzel-Giedion syndrome is characterized by severe midface retraction, multiple skull anomalies, clubfeet, and cardiac and renal malformations. ...
The Schinzel-Giedion syndrome is characterized by severe midface retraction, multiple skull anomalies, clubfeet, and ca …
Schinzel-Giedion syndrome: report of splenopancreatic fusion and proposed diagnostic criteria.
Lehman AM, McFadden D, Pugash D, Sangha K, Gibson WT, Patel MS. Lehman AM, et al. Am J Med Genet A. 2008 May 15;146A(10):1299-306. doi: 10.1002/ajmg.a.32277. Am J Med Genet A. 2008. PMID: 18398855
We report on the 46th patient with Schinzel-Giedion syndrome (SGS) and the first observation of splenopancreatic fusion in this syndrome. ...Splenopancreatic fusion, usually encountered in trisomy 13, was found on autopsy. Schinzel-Giedion sy …
We report on the 46th patient with Schinzel-Giedion syndrome (SGS) and the first observation of splenopancreatic fusion …
Three new cases of the Schinzel-Giedion syndrome and review of the literature.
Labrune P, Lyonnet S, Zupan V, Imbert MC, Goutieres F, Hubert P, Le Merrer M. Labrune P, et al. Am J Med Genet. 1994 Mar 1;50(1):90-3. doi: 10.1002/ajmg.1320500120. Am J Med Genet. 1994. PMID: 8160760 Review.
Schinzel-Giedion syndrome is rare and likely to be inherited as an autosomal recessive trait. ...Since no genetic marker is available, the prenatal diagnosis of Schinzel-Giedion syndrome relies on ultrasound examination, especially detect …
Schinzel-Giedion syndrome is rare and likely to be inherited as an autosomal recessive trait. ...Since no genetic marke …
33 results