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Infants have microcephaly with craniostenosis and dysmyelination of the brain.
It is also called craniostenosis.
SCARF syndrome is a rare syndrome characterized by skeletal abnormalities, cutis laxa, craniostenosis, ambiguous genitalia, retardation, and facial abnormalities.
Children whose cranial plates fuse too early may suffer deformities and brain damage as the skull does not expand properly to accommodate the growing brain, a condition known as craniostenosis.
Craniostenosis CSO Kleeblattschadel Deformity Plagiocephaly Trigonocephaly Turricephaly Scaphocephaly Primary Craniosynostosis is a rare disorder of the skull that may be inherited as an autosomal dominant or autosomal recessive genetic trait.
Craniofacial Dysostosis Crouzon Craniofacial Dysostosis Craniostenosis, Crouzon Type Oxycephaly-Acrocephaly Virchow's Oxycephaly Crouzon syndrome is a rare genetic disorder that may be evident at birth (congenital) or during infancy.