-
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...
-
abnormal bone
development (e.g.
craniosynostosis syndromes) and cancer. FGFR2
mutations are the
cause of
several craniosynostosis syndromes: Acrocephalosyndactyly...
- 4
Craniosynostosis (nonsyndromic) 4
Craniosynostosis and
dental anomalies Craniosynostosis-anal anomalies-porokeratosis
syndrome Craniosynostosis-Dandy-Walker...
-
Hydrocephalus is a
condition in
which cerebrospinal fluid (CSF)
builds up
within the brain,
which can
cause pressure to
increase in the skull. Symptoms...
-
Osteogenesis imperfecta (IPA: /ˌɒstioʊˈdʒɛnəsɪs ˌɪmpɜːrˈfɛktə/; OI),
colloquially known as
brittle bone disease, is a
group of
genetic disorders that all...
-
characterized by the
premature fusion of
certain bones of the
skull (
craniosynostosis),
which affects the
shape of the head and face. The
syndrome includes...
-
Muenke syndrome, also
known as FGFR3-related
craniosynostosis, is a
human specific condition characterized by the
premature closure of
certain bones of...
-
affected as well,
similar to
Crouzon syndrome and
Pfeiffer syndrome.
Craniosynostosis occurs when the
fetal skull and
facial bones fuse too soon in utero...
- 1016/s0387-7604(79)80039-x. PMID 95427. S2CID 4698879. López-Hernández, A (2013). "
Craniosynostosis, ataxia,
trigeminal anaesthesia and
parietal alopecia with pons-vermis...
- Cole-Carpenter
syndrome 2
Craniorhiny Craniosynostosis (nonsyndromic) 6
Craniosynostosis, Boston-type (nonsyndromic)
Craniosynostosis and
dental anomalies Fontaine...
