- now
known as the
Apert syndrome subtype of
acrocephalosyndactyly.
Other subtypes of
acrocephalosyndactyly were
characterized throughout the 20th century...
-
Apert syndrome is a form of
acrocephalosyndactyly, a
congenital disorder characterized by
malformations of the skull, face,
hands and feet. It is classified...
-
Pfeiffer syndrome is a rare
genetic disorder,
characterized by the
premature fusion of
certain bones of the
skull (craniosynostosis),
which affects the...
- Saethre–Chotzen
syndrome (SCS), also
known as
acrocephalosyndactyly type III, is a rare
congenital disorder ****ociated with
craniosynostosis (premature...
- syndactyly, and polydactyly.
Acrocephalopolysyndactyly is a
variation of
acrocephalosyndactyly that
presents with polydactyly. It was
first characterized in 1909...
- Jackson–Weiss
syndrome (JWS) is a
genetic disorder characterized by foot
abnormalities and the
premature fusion of
certain bones of the
skull (craniosynostosis)...
-
following conditions feature exophthalmos: 4p
partial monosomy syndrome Acrocephalosyndactyly type I
Acrofrontofacionasal dysostosis type 2 Aneurysm-osteoarthritis...
-
turricephaly include: Achondrogenesis, type IA
Acrocephalopolydactyly Acrocephalosyndactyly type V (Goodman syndrome)
Acrocraniofacial dysostosis Alopecia -...
-
Sagittal craniosynostosis is seen in many
conditions and syndromes:
Acrocephalosyndactyly type I Baller–Gerold
syndrome Cardiocranial syndrome,
Pfeiffer type...
- Albright's
hereditary osteodystrophy Angelman syndrome Apert syndrome (
acrocephalosyndactyly) Arthrogryposis–renal dysfunction–cholestasis
syndrome Ataxia telangiectasia...
