Literature DB >> 2585466

Unknown syndrome in sibs: microcephaly, seizures, mental retardation, congenital heart disease, and skeletal abnormalities.

G E Holmes1, R N Schimke.   

Abstract

We present two male sibs with a series of malformations including microcephaly, mental retardation, congenital heart disease, skeletal abnormalities, micropenis, and mild hypothyroidism. Both have had seizures. While the pattern of abnormalities is similar to that previously reported in this journal as an unknown syndrome, the facies is clearly distinct, the hypothyroidism is mild, micropenis is present, and there are additional minor skeletal abnormalities.

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Year:  1989        PMID: 2585466      PMCID: PMC1015724          DOI: 10.1136/jmg.26.10.665

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  2 in total

1.  Unknown syndrome: abnormal facies, hypothyroidism, and severe retardation: a second patient.

Authors:  J P Fryns; P Moerman
Journal:  J Med Genet       Date:  1988-07       Impact factor: 6.318

2.  Unknown syndrome: abnormal facies, congenital heart defects, hypothyroidism, and severe retardation.

Authors:  I D Young; K Simpson
Journal:  J Med Genet       Date:  1987-11       Impact factor: 6.318

  2 in total
  2 in total

1.  Continuation of a case report.

Authors:  G E Holmes; R N Schimke; K Goertz; L Mattioli; W Richardson
Journal:  J Med Genet       Date:  1993-05       Impact factor: 6.318

2.  Parental consanguinity in the blepharophimosis, heart defect, hypothyroidism, mental retardation syndrome (Young-Simpson syndrome).

Authors:  D T Bonthron; K M Barlow; A M Burt; D G Barr
Journal:  J Med Genet       Date:  1993-03       Impact factor: 6.318

  2 in total

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