We describe a 7-year-boy with severe prenatal and postnatal growth retardation, skeletal changes, normal intellect, and unusual facial appearance. The skeletal changes are suggestive of osteodysplastic primordial dwarfism type II (OPD II). He is the first patient of this kind from the Indian subcontinent and the 18th to be reported, based on a literature search (MEDLINE; 1982 to April 1997). He also represents the first case of OPD-II with normal intellect but delayed central nervous system myelination
We are reporting a very rare case of primordial dwarfism associated with lissencephaly and brain cys...
Several syndromes have been recognized with digital abnormality and CNS involvement such as oculoden...
We report two unrelated infants with cephaloskeletal dysplasia or Taybi-Linder syndrome, also referr...
Majewski osteodysplastic primordial dwarfism type II (MOPD II) is an unusual autosomal recessive inh...
A description of the clinical features of Majewski osteodysplastic primordial dwarfism type II (MOPD...
Introduction: Primordial dwarfism is a rare class of genetic disorders, characterized by intrauterin...
Osteodysplastic primordial dwarfism, type II manifests typical skeletal features which have not prev...
SUMMARY A father and son, both affected by a skeletal dysplasia with severe craniofacial deform-itie...
Primordial dwarfism refers to severely impaired growth beginning early in fetal life. There are many...
A new type of osteodysplastic primordial dwarfism is delineated in a 5- year-old female child with s...
We describe three unrelated patients with intrauterine growth retardation (IUGR) and nearly identica...
We report on a 3-year-old boy with prenatal onset of proportionate dwarfism, postnatal severe microc...
This journal suppl. is the Special Issue: Abstracts of the 24th Congress of the International Associ...
Microcephalic osteodysplastic primordial dwarfism is a syndrome characterized by the presence of int...
AbstractWe are reporting a very rare case of primordial dwarfism associated with lissencephaly and b...
We are reporting a very rare case of primordial dwarfism associated with lissencephaly and brain cys...
Several syndromes have been recognized with digital abnormality and CNS involvement such as oculoden...
We report two unrelated infants with cephaloskeletal dysplasia or Taybi-Linder syndrome, also referr...
Majewski osteodysplastic primordial dwarfism type II (MOPD II) is an unusual autosomal recessive inh...
A description of the clinical features of Majewski osteodysplastic primordial dwarfism type II (MOPD...
Introduction: Primordial dwarfism is a rare class of genetic disorders, characterized by intrauterin...
Osteodysplastic primordial dwarfism, type II manifests typical skeletal features which have not prev...
SUMMARY A father and son, both affected by a skeletal dysplasia with severe craniofacial deform-itie...
Primordial dwarfism refers to severely impaired growth beginning early in fetal life. There are many...
A new type of osteodysplastic primordial dwarfism is delineated in a 5- year-old female child with s...
We describe three unrelated patients with intrauterine growth retardation (IUGR) and nearly identica...
We report on a 3-year-old boy with prenatal onset of proportionate dwarfism, postnatal severe microc...
This journal suppl. is the Special Issue: Abstracts of the 24th Congress of the International Associ...
Microcephalic osteodysplastic primordial dwarfism is a syndrome characterized by the presence of int...
AbstractWe are reporting a very rare case of primordial dwarfism associated with lissencephaly and b...
We are reporting a very rare case of primordial dwarfism associated with lissencephaly and brain cys...
Several syndromes have been recognized with digital abnormality and CNS involvement such as oculoden...
We report two unrelated infants with cephaloskeletal dysplasia or Taybi-Linder syndrome, also referr...