Literature DB >> 953225

Syndrome of camptodactyly, multiple ankyloses, facial anomalies and pulmonary hypoplasia--further delineation and evidence for autosomal recessive inheritance.

S D Pena, M H Shokeir.   

Abstract

Entities:  

Mesh：

Year:  1976        PMID： 953225

Source DB:  PubMed          Journal:  Birth Defects Orig Artic Ser        ISSN： 0547-6844


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  6 in total

1.  Disturbances in neuronal migration and laminar cortical organization associated with multicystic encephalopathy in the Pena-Shokeir syndrome.

Authors:  B H Choi; W R Ruess; R C Kim
Journal:  Acta Neuropathol       Date:  1986       Impact factor: 17.088

2.  The syndrome of multiple ankyloses and facial anomalies. A neuropathologic analysis.

Authors:  R S Williams; L B Holmes
Journal:  Acta Neuropathol       Date:  1980       Impact factor: 17.088

3.  A diagnostic survey of infants referred for chromosome analysis in the neonatal period.

Authors:  R M Winter; M A Ridler; J A McKeown
Journal:  Br Med J       Date:  1980-10-18

Review 4.  The importance of foetal movement for co-ordinated cartilage and bone development in utero : clinical consequences and potential for therapy.

Authors:  C A Shea; R A Rolfe; P Murphy
Journal:  Bone Joint Res       Date:  2015-07       Impact factor: 5.853

5.  Arthrogryposis: an update on clinical aspects, etiology, and treatment strategies.

Authors:  Bartłomiej Kowalczyk; Jarosław Feluś
Journal:  Arch Med Sci       Date:  2016-02-02       Impact factor: 3.318

Review 6.  Pena-Shokeir syndrome: current management strategies and palliative care.

Authors:  Sumaiya Adam; Melantha Coetzee; Engela Magdalena Honey
Journal:  Appl Clin Genet       Date:  2018-10-25
  6 in total

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