TY - JOUR
T1 - Familial lethal skeletal dysplasia with cloverleaf skull and multiple anomalies of brain, eye, face and heart
T2 - A new autosomal recessive multiple congenital anomalies syndrome
AU - Sharony, R.
AU - Kidron, D.
AU - Amiel, A.
AU - Fejgin, M.
AU - Borochowitz, Z. U.
PY - 2002/5/1
Y1 - 2002/5/1
N2 - We report on a 'new' lethal familial short-limb bone dysplasia associated th multiple anomalies in three sibs born to Arabic-Muslim consanguineous healthy parents. Clinical abnormalities included short limbs and short hands, cloverleaf skull, frontal bossing, wide anterior fontanel, hypertelorism, bilateral microphthalmia, cataract, low-set ears, narrow chest, ambiguous genitalia, cardiac ventricular septal defect (VSD) and agenesis of the corpus callosum. Radiological abnormalities included cloverleaf skull, hypoplastic clavicles and scapulae, thin, wavy cupped ribs, flat vertebral bodies with coronal clefting and several unossified vertebral pedicles and hypo-ossification of the pubic bone. The main changes noted in the long bones consisted of short-bowed long bones with abnormal metaphyses and unossified epiphyses. Chondro-osseous morphology documented degenerating chondrocytes with disorganization of the hypertrophied cartilage and short disorganized columns of hypertrophied areas. An autosomal recessive mode of inheritance seems most likely.
AB - We report on a 'new' lethal familial short-limb bone dysplasia associated th multiple anomalies in three sibs born to Arabic-Muslim consanguineous healthy parents. Clinical abnormalities included short limbs and short hands, cloverleaf skull, frontal bossing, wide anterior fontanel, hypertelorism, bilateral microphthalmia, cataract, low-set ears, narrow chest, ambiguous genitalia, cardiac ventricular septal defect (VSD) and agenesis of the corpus callosum. Radiological abnormalities included cloverleaf skull, hypoplastic clavicles and scapulae, thin, wavy cupped ribs, flat vertebral bodies with coronal clefting and several unossified vertebral pedicles and hypo-ossification of the pubic bone. The main changes noted in the long bones consisted of short-bowed long bones with abnormal metaphyses and unossified epiphyses. Chondro-osseous morphology documented degenerating chondrocytes with disorganization of the hypertrophied cartilage and short disorganized columns of hypertrophied areas. An autosomal recessive mode of inheritance seems most likely.
KW - Cloverleaf skull
KW - Corpus callosum
KW - Lethal skeletal dysplasia
KW - Multiple congenital anomalies
KW - Short long bones
UR - http://www.scopus.com/inward/record.url?scp=0036590309&partnerID=8YFLogxK
U2 - 10.1034/j.1399-0004.2002.610509.x
DO - 10.1034/j.1399-0004.2002.610509.x
M3 - ???researchoutput.researchoutputtypes.contributiontojournal.shortsurvey???
AN - SCOPUS:0036590309
SN - 0009-9163
VL - 61
SP - 369
EP - 374
JO - Clinical Genetics
JF - Clinical Genetics
IS - 5
ER -