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Prenatal sonographic diagnosis of Grebe syndrome.
Cordero DR, Goldberg Y, Basel D, Kilpatrick MW, Klugman S, Tsipouras P, Gross S. Cordero DR, et al. J Ultrasound Med. 2006 Jan;25(1):115-8; quiz 119-21. doi: 10.7863/jum.2006.25.1.115. J Ultrasound Med. 2006. PMID: 16371562 No abstract available.
Grebe syndrome: clinical and radiographic findings in affected individuals and heterozygous carriers.
Costa T, Ramsby G, Cassia F, Peters KR, Soares J, Correa J, Quelce-Salgado A, Tsipouras P. Costa T, et al. Am J Med Genet. 1998 Feb 17;75(5):523-9. doi: 10.1002/(sici)1096-8628(19980217)75:5<523::aid-ajmg13>3.0.co;2-m. Am J Med Genet. 1998. PMID: 9489798
Grebe syndrome is a recessively inherited acromesomelic dysplasia. ...Heterozygotes presented with a variety of skeletal manifestations including polydactyly, brachydactyly, hallux valgus, and metatarsus adductus. Grebe syndrome is caused by a missense …
Grebe syndrome is a recessively inherited acromesomelic dysplasia. ...Heterozygotes presented with a variety of skeletal manif …
Grebe syndrome with bilateral fibular hemimelia and thumb duplication.
Rao N, Joseph B. Rao N, et al. Skeletal Radiol. 2002 Mar;31(3):183-7. doi: 10.1007/s00256-001-0461-0. Epub 2002 Jan 23. Skeletal Radiol. 2002. PMID: 11935206
Grebe syndrome is a rare recessively inherited form of short-limbed dwarfism. Among the skeletal anomalies reported in the past, complete fibular hemimelia and thumb duplication have not been documented. We report a case of Grebe syndrome with these as …
Grebe syndrome is a rare recessively inherited form of short-limbed dwarfism. Among the skeletal anomalies reported in the pas …
Characterization of an acromesomelic dysplasia, Grebe type case: novel mutation affecting the recognition motif at the processing site of GDF5.
Martinez-Garcia M, Garcia-Canto E, Fenollar-Cortes M, Aytes AP, Trujillo-Tiebas MJ. Martinez-Garcia M, et al. J Bone Miner Metab. 2016 Sep;34(5):599-603. doi: 10.1007/s00774-015-0693-z. Epub 2015 Aug 15. J Bone Miner Metab. 2016. PMID: 26275437
Acromesomelic dysplasia, Grebe type is a very rare skeletal dysplasia characterized by severe dwarfism with marked micromelia and deformation of the upper and lower limbs, with a proximodistal gradient of severity. CDMP1 gene mutations have been associated with Grebe sy …
Acromesomelic dysplasia, Grebe type is a very rare skeletal dysplasia characterized by severe dwarfism with marked micromelia and deformatio …
Heterogeneity of nonlethal severe short-limbed dwarfism.
Romeo G, Zonana J, Rimoin DL, Lachman RS, Scott CI Jr, Kaveggia EG, Spranger JW, Opitz JM. Romeo G, et al. J Pediatr. 1977 Dec;91(6):918-23. doi: 10.1016/s0022-3476(77)80890-1. J Pediatr. 1977. PMID: 925797
The Grebe syndrome is a nonlethal form of severe short-limbed dwarfism which was previously called "achondrogenesis-Brazilian or Grebe type". ...
The Grebe syndrome is a nonlethal form of severe short-limbed dwarfism which was previously called "achondrogenesis-Brazilian …
Grebe syndrome: a rare association with congenital heart disease.
Jalil J, Shafique M, Ehtesham-ul-Haq. Jalil J, et al. J Coll Physicians Surg Pak. 2012 Apr;22(4):261-3. J Coll Physicians Surg Pak. 2012. PMID: 22482388
Grebe syndrome is a very rare form of short-limbed dwarfism. It is a genetic condition, passed by autosomal recessive inheritance. ...The affected baby has normal intelligence and normal life span. We present here a case of Grebe syndrome along with co …
Grebe syndrome is a very rare form of short-limbed dwarfism. It is a genetic condition, passed by autosomal recessive inherita …