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Aprosencephaly
Known as:
Aprosencephalies
A very rare congenital brain defect in which the cerebral cortex, striatum, globus pallidus, thalamus, hypothalamus, and eyes are absent or…
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National Institutes of Health
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Related topics
Related topics
2 relations
Broader (1)
Anencephaly
Congenital neurologic anomalies
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2012
2012
Aprosencephaly with Otocephaly in a Lamb (Ovis aries)
L. Brachthäuser
,
S. Klumpp
,
+4 authors
Christiane Herden
Veterinary Pathology-Supplement
2012
Corpus ID: 7294365
Aprosencephaly is a rare condition in veterinary and human medicine characterized by the complete absence of telencephalon and…
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2001
2001
Aprosencephaly: histopathological features of the rudimentary forebrain and retina
A. Kakita
,
S. Hayashi
,
M. Arakawa
,
H. Takahashi
Acta Neuropathologica
2001
Corpus ID: 27547492
Abstract. Aprosencephaly/atelencephaly is an extremely rare central nervous system defect of the human fetus, which has been…
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2000
2000
The vesicular forebrain (pseudo-aprosencephaly): a missing link in the teratogenetic spectrum of the defective brain anlage and its discrimination from aprosencephaly
C. Sergi
,
H. Schmitt
Acta Neuropathologica
2000
Corpus ID: 29372703
Abstract Two cases out of a sample of 41 fetuses and infants with prosencephalic malformation, observed at the Institute of…
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Review
1998
Review
1998
XK aprosencephaly.
L. Al-Gazali
,
D. Bakalinova
,
M. Bakir
,
K. Nath
Clinical Dysmorphology
1998
Corpus ID: 36849027
We report a baby with aprosencephaly, preaxial limb defect and ambiguous genitalia. This combination of abnormalities have been…
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1998
1998
Congenital anomalies in the teratological collection of Museum Vrolik in Amsterdam, The Netherlands. III: primary field defects, sequences, and other complex anomalies.
R. Oostra
,
B. Baljet
,
B. Verbeeten
,
R. Hennekam
American journal of medical genetics
1998
Corpus ID: 29070862
The Museum Vrolik collection of the Department of Anatomy and Embryology of the Academic Medical Center, University of Amsterdam…
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Review
1996
Review
1996
Aprosencephaly and cerebellar dysgenesis in sibs.
S. Florell
,
Jeannette J. Townsend
,
+4 authors
David Viskochil
American journal of medical genetics
1996
Corpus ID: 36946479
Aprosencephaly is a rare, lethal malformation sequence of the central nervous system that has been attributed to a…
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1993
1993
Mosaic r(13) in an infant with aprosencephaly.
C. Goldsmith
,
G. Tawagi
,
B. Carpenter
,
M. Speevak
,
A. Hunter
American journal of medical genetics
1993
Corpus ID: 46322170
We report on a stillborn male infant with a mosaic ring 13 karyotype (45,XY,-13/46,XY,-13,+r(13)) with apparent aprosencephaly…
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Review
1982
Review
1982
A review and case report of aprosencephaly and the XK aprosencephaly syndrome.
R. Martin
,
J. Carey
American journal of medical genetics
1982
Corpus ID: 40864258
1979
1979
Sporadic case of apparent aprosencephaly.
W. Adkins
,
E. Kaveggia
American journal of medical genetics
1979
Corpus ID: 41273062
We report a sporadic case of apparent aprosencephaly, ie, apparent absence of forebrain with the facial anomalies of the (alobar…
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1979
1979
Brief clinical reports: aprosencephaly-atelencephaly and the aprosencephaly (XK) syndrome.
I. Lurie
,
M. Nedzved
,
G. Lazjuk
,
I. Kirillova
,
E. Cherstvoy
American journal of medical genetics
1979
Corpus ID: 22113596
We report on a postnatally dead, postterm male infant with aprosencephaly and the oculofacial manifestations usually seen in the…
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