-
Nager acrofacial dysostosis, also
known as
Nager syndrome, is a
genetic disorder which displays several or all of the
following characteristics: underdevelopment...
-
Acrodysplasia scoliosis Acrofacial dysostosis Acrofacial dysostosis ambiguous genitalia Acrofacial dysostosis atypical postaxial Acrofacial dysostosis Catania...
-
monosomy syndrome Achard syndrome Acrofacial dysostosis Cincinnati type
Acrofacial dysostosis Rodriguez type
Acrofacial dysostosis,
Catania type Acromegaloid...
- as Genée–Wiedemann syndrome, Wildervanck–Smith
syndrome or
postaxial acrofacial dysostosis, is an
extremely rare
genetic condition that
manifests as craniofacial...
- vitiligo: one or a few
scattered macules in one area, most
common in
children Acrofacial vitiligo:
fingers and
periorificial areas Mucosal vitiligo: depigmentation...
-
syndrome (8q13
microdeletion syndrome)
Microgastria Myhre syndrome Nager acrofacial dysostosis Neu–Laxova
syndrome Patau syndrome Pfeiffer syndrome Poland...
- Anthropology. 144 (3): 432–41. doi:10.1002/ajpa.21424. PMID 21302269. "Weyers
acrofacial dysostosis / "Genetics Home Reference" ("Your
Guide to
Understanding Genetic...
-
Vascular disruption during fetal development Differential diagnosis Nager acrofacial dysostosis Johnson Hall
Krous syndrome Goldenhar syndrome Frequency <1/1...
- Meckel–Gruber
syndrome and some
forms of
retinal degeneration.
Weyers acrofacial dysostosis is due to
another mutation in the EVC gene and
hence is allelic...
- and
other chromosome disorders (e.g., 4p- syndrome,
Williams syndrome),
acrofacial dysostosis, Antley–Bixler syndrome,
genitopatellar syndrome,
Greig cephalopolysyndactyly...