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Fallot complex, severe mental, and growth retardation: a new autosomal recessive syndrome?
Am J Med Genet. 1994 Apr 01; 50(2):173-6.AJ

Abstract

We report on the syndromic occurrence of the Fallot complex in sibs born to consanguineous Pakistani parents. Additional manifestations included minor facial anomalies, pronounced failure to thrive, and mental retardation. Expression of the syndrome varied. While one of the four patients had cardiac malformations, another sib had only non-cardiac manifestations. The clinical findings suggest a new autosomal recessive syndrome.

Authors+Show Affiliations

Institut für Humangenetik, Justus-Liebig Universität Giessen, Germany.No affiliation info availableNo affiliation info available

Pub Type(s)

Case Reports
Journal Article

Language

eng

PubMed ID

8010348

Citation

Bindewald, B, et al. "Fallot Complex, Severe Mental, and Growth Retardation: a New Autosomal Recessive Syndrome?" American Journal of Medical Genetics, vol. 50, no. 2, 1994, pp. 173-6.
Bindewald B, Ulmer H, Müller U. Fallot complex, severe mental, and growth retardation: a new autosomal recessive syndrome? Am J Med Genet. 1994;50(2):173-6.
Bindewald, B., Ulmer, H., & Müller, U. (1994). Fallot complex, severe mental, and growth retardation: a new autosomal recessive syndrome? American Journal of Medical Genetics, 50(2), 173-6.
Bindewald B, Ulmer H, Müller U. Fallot Complex, Severe Mental, and Growth Retardation: a New Autosomal Recessive Syndrome. Am J Med Genet. 1994 Apr 1;50(2):173-6. PubMed PMID: 8010348.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Fallot complex, severe mental, and growth retardation: a new autosomal recessive syndrome? AU - Bindewald,B, AU - Ulmer,H, AU - Müller,U, PY - 1994/4/1/pubmed PY - 1994/4/1/medline PY - 1994/4/1/entrez SP - 173 EP - 6 JF - American journal of medical genetics JO - Am J Med Genet VL - 50 IS - 2 N2 - We report on the syndromic occurrence of the Fallot complex in sibs born to consanguineous Pakistani parents. Additional manifestations included minor facial anomalies, pronounced failure to thrive, and mental retardation. Expression of the syndrome varied. While one of the four patients had cardiac malformations, another sib had only non-cardiac manifestations. The clinical findings suggest a new autosomal recessive syndrome. SN - 0148-7299 UR - https://www.unboundmedicine.com/medline/citation/8010348/Fallot_complex_severe_mental_and_growth_retardation:_a_new_autosomal_recessive_syndrome L2 - https://onlinelibrary.wiley.com/resolve/openurl?genre=article&sid=nlm:pubmed&issn=0148-7299&date=1994&volume=50&issue=2&spage=173 DB - PRIME DP - Unbound Medicine ER -