Background: Microcephaly-capillary malformation (MIC-CAP) syndrome is a newly described autosomal recessive syndrome characterized by microcephaly, multiple cutaneous capillary malformations, intractable epilepsy and profound developmental delay. We present the first description of MIC-CAP syndrome in Russia.Patient: We describe a 6-month-old girl with severe congenital microcephaly, intractable epilepsy (infantile spasms), multiple cutaneous capillary malformations and facial abnormalities. Genetic studies revealed the presence of new STAMPB gene mutations in the compound heterozygous state: c.273delA and the intron replacement c.204-5 C > G.Conclusions: This report presents a case of MIC-CAP syndrome with earlier unreported new mutatio...
Hennekam syndrome is a rare autosomal recessive disorder resulting from malformation of the lymphati...
The article focuses on the problematic of Möbius syndrome, a specific description of a child with th...
Holoprosencephaly is a common developmental defect of the forebrain and midface in humans. Clinical ...
Microcephaly-capillary malformation is a relatively new syndrome, which has been reported since 2011...
Megalencephaly-capillary malformation-polymicrogyria syndrome (MCAP), previously known as macrocepha...
Microcephaly–capillary malformation (MIC-CAP) syndrome is characterized by severe microcephaly with ...
Background: Autosomal recessive defects of either the B1, E1, M1 or S1 subunit of the Adaptor Protei...
We are reporting a very rare case of primordial dwarfism associated with lissencephaly and brain cys...
AbstractWe report two individual cases of cardio-facio-cutaneous (CFC) syndrome with severe neurolog...
As a rare multisystem congenital anomaly disorder, Cornelia de Lange syndrome (CdLS) is featured by ...
Cornelia de Lange syndrome is a developmental disorder that affects many parts of the body. The firs...
BACKGROUND: Autosomal recessive primary microcephaly (MCPH) is a rare neurodevelopmental disease wit...
Introduction and Aim: Microcephaly is described as a head circumference more than two standard devia...
Megalencephaly capillary malformation polymicrogyria (MCAP) syndrome is characterized by the sporadi...
The International University of Andalucía (UNIA) Current Trends in Biomedicine Workshop on Molecular...
Hennekam syndrome is a rare autosomal recessive disorder resulting from malformation of the lymphati...
The article focuses on the problematic of Möbius syndrome, a specific description of a child with th...
Holoprosencephaly is a common developmental defect of the forebrain and midface in humans. Clinical ...
Microcephaly-capillary malformation is a relatively new syndrome, which has been reported since 2011...
Megalencephaly-capillary malformation-polymicrogyria syndrome (MCAP), previously known as macrocepha...
Microcephaly–capillary malformation (MIC-CAP) syndrome is characterized by severe microcephaly with ...
Background: Autosomal recessive defects of either the B1, E1, M1 or S1 subunit of the Adaptor Protei...
We are reporting a very rare case of primordial dwarfism associated with lissencephaly and brain cys...
AbstractWe report two individual cases of cardio-facio-cutaneous (CFC) syndrome with severe neurolog...
As a rare multisystem congenital anomaly disorder, Cornelia de Lange syndrome (CdLS) is featured by ...
Cornelia de Lange syndrome is a developmental disorder that affects many parts of the body. The firs...
BACKGROUND: Autosomal recessive primary microcephaly (MCPH) is a rare neurodevelopmental disease wit...
Introduction and Aim: Microcephaly is described as a head circumference more than two standard devia...
Megalencephaly capillary malformation polymicrogyria (MCAP) syndrome is characterized by the sporadi...
The International University of Andalucía (UNIA) Current Trends in Biomedicine Workshop on Molecular...
Hennekam syndrome is a rare autosomal recessive disorder resulting from malformation of the lymphati...
The article focuses on the problematic of Möbius syndrome, a specific description of a child with th...
Holoprosencephaly is a common developmental defect of the forebrain and midface in humans. Clinical ...