Literature DB >> 3172145

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

J P Fryns1, P Moerman.   

Abstract

In the November 1987 issue of this journal, Young and Simpson presented a female infant with abnormal facies (microcephaly, blepharophimosis, small, low set, posteriorly rotated ears, bulbous nose, carp shaped mouth, and micrognathia), congenital heart abnormalities (large atrial and ventricular septal defects), congenital hypothyroidism, and severe global retardation. We have observed a male newborn with a similar pattern of malformations (figs. 1 and 2).

Entities:  

Mesh:

Year:  1988        PMID: 3172145      PMCID: PMC1050529          DOI: 10.1136/jmg.25.7.498

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


  5 in total

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

Authors:  G E Holmes; R N Schimke
Journal:  J Med Genet       Date:  1989-10       Impact factor: 6.318

2.  Blepharophimosis-mental retardation syndrome and terminal deletion of chromosome 3p.

Authors:  A Moncla; N Philip; J F Mattei
Journal:  J Med Genet       Date:  1995-03       Impact factor: 6.318

3.  Unknown syndrome: abnormal facies, hypothyroidism, postaxial polydactyly, and severe retardation: a third patient.

Authors:  D P Cavalcanti
Journal:  J Med Genet       Date:  1989-12       Impact factor: 6.318

4.  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

Review 5.  Role of thyroid hormones in craniofacial development.

Authors:  Victoria D Leitch; J H Duncan Bassett; Graham R Williams
Journal:  Nat Rev Endocrinol       Date:  2020-01-23       Impact factor: 43.330

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.