-
Shprintzen–Goldberg
syndrome is a
congenital multiple-anomaly
syndrome that has craniosynostosis,
multiple abdominal hernias,
cognitive impairment, and...
- conditions.
These original classifications included velocardiofacial syndrome,
Shprintzen syndrome,
DiGeorge sequence/syndrome,
Sedlackova syndrome, and conotruncal...
- Goldberg–
Shprintzen syndrome is a very rare
connective tissue condition ****ociated with
mutations in KIAA1279 gene
which encodes KIF-binding
protein (KBP)...
-
Attitudes toward **** in
Antebellum America, 2006, See
specific pages.
Shprintzen, Adam D. (2013). The
Vegetarian Crusade: The Rise of an
American Reform...
-
ptosis (droopy eyelids), and
fingers maybe abnormally short and webbed.
Shprintzen-Goldberg syndrome:
craniosynostosis with
marfanoid habitus and tissue...
-
years and 1 month.
Differential diagnosis Smith Lemli Opitz syndrome,
Angelman syndrome,
Goldberg Shprintzen megacolon syndrome Treatment Supportive care...
- Schwartz-Jampel
syndrome type 1
Seckel syndrome 1, 2, 5, 8, and 9
SHORT syndrome Shprintzen-Goldberg
syndrome Silver-Russell
syndrome 1 and 2 Smith-Lemli-Opitz syndrome...
-
recessive 2 Rubinstein-Taybi
syndrome due to
CREBBP mutations Sclerosteosis 1
Shprintzen-Goldberg
syndrome Spondyloepimetaphyseal dysplasia with
joint laxity,...
- and
neurodevelopmental syndrome Fontaine progeroid syndrome Goldberg-
Shprintzen megacolon syndrome Growth delay due to insulin-like
growth factor I resistance...
- /ʃpr/, /ʃtr/ (in
words such as schlep, spiel, shtick, ****, schnapps,
Shprintzen's, strudel). /ʃw/ is
found initially in the
Hebrew loanword schwa. Before...
