Literature DB >> 1218241

Lethal faciocardiomelic dysplasia- a new autosomal recessive disorder.

J M Cantú, A Hernández, J Ramírez, M Bernal, G Rubio, J Urrusti, S Franco-Vázquez.   

Abstract

Three male sibs from consanguienous parents were found to have a strikingly similar pattern of multiple congenital anomalies. The main features were polyhydramnios; low birthweight; dwarfism; epicanthal folds; abnormal ears; microretrognathia; microstomia; microglossia; glossoptosis; webbed neck; severe cardiac defects; radial and ulnar hypoplasia; radial deviation of the hands; brachymetacarpalia; thumb hypoplasia; clinodactyly and hypoplasia of the 5th finger; simian creases; fibular and tibial hypoplasia; talipes varus with hypoplastic heels; wide gap between 1st and 2nd toes; and delayed bone age. Neonatal death occurred in the 3 babies by severe cardiac failure. Differential diagnosis permits one to conclude that this is a new type of faciocardiomelic dysplasia with a probable autosomal recessive inheritance.

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Year:  1975        PMID: 1218241

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


  2 in total

1.  Weyers' ulnar ray/oligodactyly syndrome and the association of midline malformations with ulnar ray defects.

Authors:  P D Turnpenny; J C Dean; P Duffty; J A Reid; P Carter
Journal:  J Med Genet       Date:  1992-09       Impact factor: 6.318

2.  A new lethal syndrome with cloudy corneae, diaphragmatic defects and distal limb deformities.

Authors:  J P Fryns; F Moerman; P Goddeeris; C Bossuyt; H Van den Berghe
Journal:  Hum Genet       Date:  1979       Impact factor: 4.132

  2 in total

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