Tetra-oligodactyly with bilateral aplasia and hypoplasia of long bones of upper and lower limbs: a variable manifestation of the syndrome of ectrodactyly with tibial aplasia.
Pediatr Radiol
; 21(1): 57-61, 1990.
Article
en En
| MEDLINE
| ID: mdl-2287543
We present, a family manifesting a variation of the syndrome of ectrodactyly with tibial apasia. The principal case in the family showed the most severe bilateral skeletal malformations of this syndrome. The hand changes of this case (tetra-oligodactyly with missing 5th rays) and of a relative (oligodactyly with the last 3 rays being affected) reflected a variable manifestation of "ectrodactyly". Additionally, a review of the relevant literature is presented for further delineation of various aspects of this syndrome.
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Colección:
01-internacional
Base de datos:
MEDLINE
Asunto principal:
Huesos
/
Dedos del Pie
/
Dedos
Límite:
Adult
/
Humans
/
Male
Idioma:
En
Revista:
Pediatr Radiol
Año:
1990
Tipo del documento:
Article
País de afiliación:
Turquía
Pais de publicación:
Alemania