¿Cuál es la causa del síndrome Cornelia de Lange? These cards highlight routine care for people with CdLS needed by specific age groups, including infancy, early and late childhood, adolescence and adulthood. ¿Qué cuidados Introdução: A síndrome de Cornelia de Lange (SCdL) corresponde a uma condição rara caracterizada por mutações nos genes responsáveis pelas proteínas estruturais e El síndrome de Cornelia de Lange es una enfermedad genética caracterizada por rasgos faciales distintivos, falla de medro, microcefalia y varias malformaciones asociadas. Sus ¿Qué es el Síndrome Cornelia de Lange? At each age, individuals with CdLS will have specific health care needs. El síndrome recibe el nombre de la pediatra holandesa Cornelia de Lange, que describió el trastorno por primera vez en (1) Cornelia de Lange syndrome (CdLS) encompasses a spectrum of findings from mild to severe. A rare multiple congenital anomalies syndrome characterized by facial dysmorphism, hypertrichosis, mild to profound intellectual disability, intrauterine growth restriction Cornelia de Lange is a genetic syndrome which affects between 1/ and 1/ neonates, but its genetic bases are still not clear. Its principal clinical characteristics are ¿Qué es el síndrome de Cornelia de Lange? El Síndrome Cornelia de Lange (SCdL) es una enfermedad rara del desarrollo que está presente desde el nacimiento. Severe (classic) CdLS is characterized by distinctive facial features, growth restriction (prenatal onset; <5th centile throughout life), hypertrichosis, and upper-limb reduction defects that range from subtle phalangeal abnormalities to oligodactyly Management and Treatment Guidelines for Cornelia de Lange Syndrome. Please contact the CdLS Foundation at Cornelia de Lange syndrome (CdLS) is an archetypical genetic syndrome that is characterized by intellectual disability, well-defined facial features, upper limb anomalies and atypical Cornelia de Lange syndrome (CdLS) is an archetypical genetic syndrome that is characterized by intellectual disability, well-defined facial features, upper limb anomalies and atypical growth, among numerous other signs and symptoms ¿Cómo se diagnostica el síndrome Cornelia de Lange?
¿Cuál es la causa del síndrome Cornelia de Lange? These cards highlight routine care for people with CdLS needed by specific age groups, including infancy, early and late childhood, adolescence and adulthood. ¿Qué cuidados Introdução: A síndrome de Cornelia de Lange (SCdL) corresponde a uma condição rara caracterizada por mutações nos genes responsáveis pelas proteínas estruturais e El síndrome de Cornelia de Lange es una enfermedad genética caracterizada por rasgos faciales distintivos, falla de medro, microcefalia y varias malformaciones asociadas. Sus ¿Qué es el Síndrome Cornelia de Lange? At each age, individuals with CdLS will have specific health care needs. El síndrome recibe el nombre de la pediatra holandesa Cornelia de Lange, que describió el trastorno por primera vez en (1) Cornelia de Lange syndrome (CdLS) encompasses a spectrum of findings from mild to severe. A rare multiple congenital anomalies syndrome characterized by facial dysmorphism, hypertrichosis, mild to profound intellectual disability, intrauterine growth restriction Cornelia de Lange is a genetic syndrome which affects between 1/ and 1/ neonates, but its genetic bases are still not clear. Its principal clinical characteristics are ¿Qué es el síndrome de Cornelia de Lange? El Síndrome Cornelia de Lange (SCdL) es una enfermedad rara del desarrollo que está presente desde el nacimiento. Severe (classic) CdLS is characterized by distinctive facial features, growth restriction (prenatal onset; <5th centile throughout life), hypertrichosis, and upper-limb reduction defects that range from subtle phalangeal abnormalities to oligodactyly Management and Treatment Guidelines for Cornelia de Lange Syndrome. Please contact the CdLS Foundation at Cornelia de Lange syndrome (CdLS) is an archetypical genetic syndrome that is characterized by intellectual disability, well-defined facial features, upper limb anomalies and atypical Cornelia de Lange syndrome (CdLS) is an archetypical genetic syndrome that is characterized by intellectual disability, well-defined facial features, upper limb anomalies and atypical growth, among numerous other signs and symptoms ¿Cómo se diagnostica el síndrome Cornelia de Lange?
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