Robinow syndrome
(redirected from Fetal facies syndrome)Rob·i·now syn·drome
(rob'i-now), [MIM*180700]a skeletal dysplasia characterized by bulging forehead, hypertelorism, depressed nasal bridge (so-called fetal face), wide mouth, acromesomelic shortening of limbs, hemivertebrae, and hypoplastic genitalia; there is also an autosomal recessive form [MIM*268310].
See also: fetal face syndrome.
See also: fetal face syndrome.
Synonym(s): Robinow dwarfism
Farlex Partner Medical Dictionary © Farlex 2012
Robinow syndrome
An autosomal dominant disorder (OMIM:180700) characterised by short-limb dwarfism, costovertebral segmentation defects and malformations of the head, face and external genitalia.Molecular pathology
Defects of WNT5A, which encodes a signalling molecule that regulates cell fate and patterning during embryogenesis, cause Robinow syndrome.
Segen's Medical Dictionary. © 2012 Farlex, Inc. All rights reserved.
Rob·i·now syn·drome
(rob'i-now sin'drōm)Skeletal dysplasia characterized by bulging forehead, hypertelorism, depressed nasal bridge (so-called fetal face), wide mouth, acromesomelic shortening of limbs, hemivertebrae, and hypoplastic genitalia; there is also an autosomal recessive form.
Medical Dictionary for the Health Professions and Nursing © Farlex 2012
Robinow,
Meinhard, U.S. physician, 1909–.Robinow dwarfism - Synonym(s): Robinow syndrome
Robinow mesomelic dysplasia
Robinow syndrome - dwarfism associated with several facial anomalies. Synonym(s): fetal face syndrome; Robinow dwarfism
Medical Eponyms © Farlex 2012
Rob·i·now syn·drome
(rob'i-now sin'drōm) [MIM*180700]Skeletal dysplasia characterized by bulging forehead, hypertelorism, depressed nasal bridge (so-called fetal face), and wide mouth.
Medical Dictionary for the Dental Professions © Farlex 2012