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Crouzon syndrome is an
autosomal dominant genetic disorder known as a
branchial arch syndrome. Specifically, this
syndrome affects the
first branchial...
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Louis Édouard
Octave Crouzon (1874–1938) was a
French neurologist born in Paris. He
received his
doctorate from the
University of Paris,
where he studied...
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craniofrontonasal dysplasia,
Noonan syndrome, neurofibromatosis,
LEOPARD syndrome,
Crouzon syndrome, Wolf–Hirschhorn syndrome, Andersen–Tawil syndrome, Waardenburg...
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syndrome 1
Craniosynostosis 4
Craniosynostosis and
dental anomalies Crouzon syndrome Crouzon syndrome-acanthosis
nigricans syndrome Cutis laxa,
autosomal recessive...
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Basal cell
nevus syndrome Congenital syphilis Cleidocranial dysostosis Crouzon syndrome Cryopyrin-****ociated
Periodic Syndrome (CAPS – PFS) Ectodermal...
- (1995). "Identical
mutations in the FGFR2 gene
cause both
Pfeiffer and
Crouzon syndrome phenotypes". Nat Genet. 9 (2): 173–6. doi:10.1038/ng0295-173....
- needed]
Dolichocephaly can
sometimes be a
symptom of
Sensenbrenner syndrome,
Crouzon syndrome,
Sotos syndrome,
CMFTD and
Marfan syndrome. However, it also occurs...
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combined Apert (ASC type I),
Crouzon (ASC type II), and
Pfeiffer (ASC type V)
syndrome into Apert-
Crouzon and
Crouzon-Pfeiffer syndrome. Acrocephalosyndactyly...
- the
premature fusion of all sutures. It
should be
differentiated from
Crouzon syndrome.
Oxycephaly (or acrocephaly) is a form of
turricephaly where the...
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fingers and toes fuses. The
cranial bones are
affected as well,
similar to
Crouzon syndrome and
Pfeiffer syndrome.
Craniosynostosis occurs when the fetal...
