Asymmetric neonatal crying is a rare minor congenital abnormality caused by unilateral agenesis or hypoplasia of depressor anguli oris muscle and depressor labii inferioris muscle. It is either an isolated clinical finding or one of the clinical findings included in several malformation syndromes linked to a microdeletion within a chromosomal region 22q11.2. Some malformations in that region are associated with serious cardiovascular anomalies. Nowadays, standard diagnostic techniques for detecting aberrations within the chromosomal region 22q11.2 are fluorescence in situ hybridization (FISH) and multiplex ligation probe amplification (MLPA). This short report describes an eutrophic female newborn whose both lip corners are symmetrically po...
Congenital malformations are single or multiple defects of the morphogenesis of organs or body distr...
DiGeorge syndrome (DGS) which is also known as velocardiofacial syndrome is caused by a submicroscop...
Recent studies report a high incidence of monozygotic twinning in Beckwith–Wiedemann syndrome. A phe...
Asymmetric neonatal crying is a rare minor congenital abnormality caused by unilateral agenesis or h...
Asymmetric crying facies is caused by congenital hypoplasia or agenesis of the depressor anguli oris...
Congenital asymmetric crying facies, a minor congenital anomaly due to unilateral absence or hypopla...
Asymmetric crying facies is a common neonatal problem with multiple causes. Asymmetric crying facies...
Collodion baby is a distinct subset of neonatal erythroderma that can be a clinical marker for a var...
Fetuses with 22q11.2 microdeletions (del22q11.2) have variable clinical expressions. Associated cong...
Facial asymmetry in a crying newborn can be due to a variety of different causes. Neonatal asymmetri...
DiGeorge syndrome or 22q11.2 deletion syndrome (22q11.2 DS) is the most common chromosomal microdele...
Congenital asymmetric crying facies, a minor congenital anomaly due to absence or hypoplasia of the ...
Facial asymmetry in a crying newborn can be due to a variety of different causes. Neonatal asymmetri...
Despite modern approaches in molecular biology and genetics, we are still not able to identify the a...
We describe an additional newborn with craniofacial dysmorphisms, congenital heart disease, hypotoni...
Congenital malformations are single or multiple defects of the morphogenesis of organs or body distr...
DiGeorge syndrome (DGS) which is also known as velocardiofacial syndrome is caused by a submicroscop...
Recent studies report a high incidence of monozygotic twinning in Beckwith–Wiedemann syndrome. A phe...
Asymmetric neonatal crying is a rare minor congenital abnormality caused by unilateral agenesis or h...
Asymmetric crying facies is caused by congenital hypoplasia or agenesis of the depressor anguli oris...
Congenital asymmetric crying facies, a minor congenital anomaly due to unilateral absence or hypopla...
Asymmetric crying facies is a common neonatal problem with multiple causes. Asymmetric crying facies...
Collodion baby is a distinct subset of neonatal erythroderma that can be a clinical marker for a var...
Fetuses with 22q11.2 microdeletions (del22q11.2) have variable clinical expressions. Associated cong...
Facial asymmetry in a crying newborn can be due to a variety of different causes. Neonatal asymmetri...
DiGeorge syndrome or 22q11.2 deletion syndrome (22q11.2 DS) is the most common chromosomal microdele...
Congenital asymmetric crying facies, a minor congenital anomaly due to absence or hypoplasia of the ...
Facial asymmetry in a crying newborn can be due to a variety of different causes. Neonatal asymmetri...
Despite modern approaches in molecular biology and genetics, we are still not able to identify the a...
We describe an additional newborn with craniofacial dysmorphisms, congenital heart disease, hypotoni...
Congenital malformations are single or multiple defects of the morphogenesis of organs or body distr...
DiGeorge syndrome (DGS) which is also known as velocardiofacial syndrome is caused by a submicroscop...
Recent studies report a high incidence of monozygotic twinning in Beckwith–Wiedemann syndrome. A phe...