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Short stature, brachydactyly, and Peters' anomaly (Peters'-plus syndrome): confirmation of autosomal recessive inheritance.
de Almeida, J C; Reis, D F; Llerena Júnior, J; Barbosa Neto, J; Pontes, R L; Middleton, S; Telles, L F.
Affiliation
  • de Almeida JC; Centro de Genética Médica, Instituto Fernandes Figueira, Rio de Janeiro, Brazil.
J Med Genet ; 28(4): 277-9, 1991 Apr.
Article in En | MEDLINE | ID: mdl-1856836
ABSTRACT
Two sibs with a phenotype characterised by short stature, brachydactyly, and ocular anomalies (Peters' anomaly) are reported (Peters'-plus syndrome). The consanguinity is in agreement with the proposed autosomal recessive inheritance.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cornea / Genes, Recessive / Growth Disorders Limits: Child, preschool / Female / Humans / Infant / Male Language: En Journal: J Med Genet Year: 1991 Document type: Article Affiliation country: Brazil
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cornea / Genes, Recessive / Growth Disorders Limits: Child, preschool / Female / Humans / Infant / Male Language: En Journal: J Med Genet Year: 1991 Document type: Article Affiliation country: Brazil