-
combined with a
significant reduction in IQ.
Craniosynostosis occurs in one in 2000 births.
Craniosynostosis is part of a
syndrome in 15% to 40% of affected...
-
affected as well,
similar to
Crouzon syndrome and
Pfeiffer syndrome.
Craniosynostosis occurs when the
fetal skull and
facial bones fuse too soon in utero...
- 4
Craniosynostosis (nonsyndromic) 4
Craniosynostosis and
dental anomalies Craniosynostosis-anal anomalies-porokeratosis
syndrome Craniosynostosis-Dandy-Walker...
-
enough space for the
growing brain,
craniosynostosis results in
increased intracranial pressure.
Craniosynostosis is
called simple when one
suture is...
- and Dandy-Walker malformation.
Hydrocephalus can also
occur with
craniosynostosis,
being a
constant feature of Kleeblattschädel and
frequently seen in...
-
Osteogenesis imperfecta (IPA: /ˌɒstioʊˈdʒɛnəsɪs ˌɪmpɜːrˈfɛktə/; OI),
colloquially known as
brittle bone disease, is a
group of
genetic disorders that all...
- Cole-Carpenter
syndrome 2
Craniorhiny Craniosynostosis (nonsyndromic) 6
Craniosynostosis, Boston-type (nonsyndromic)
Craniosynostosis and
dental anomalies Fontaine...
-
characterized by the
premature fusion of
certain bones of the
skull (
craniosynostosis),
which affects the
shape of the head and face. The
syndrome includes...
-
condition and can
range from minor, single-suture
craniosynostosis to major,
multisutural craniosynostosis. "3MC
syndrome 2 (Concept Id: C0796279)". www.ncbi...
- Shprintzen–Goldberg
syndrome is a
congenital multiple-anomaly
syndrome that has
craniosynostosis,
multiple abdominal hernias,
cognitive impairment, and
other skeletal...
