- syndrome) and is
thought to
belong to a
family of
oromandibular limb
hypogenesis syndrome (OLHS). It is
believed to be
caused by heat-induced vascular...
-
defects exist,
including hypoplasia (underdevelopment or thinness),
hypogenesis (partial agenesis) or
dysgenesis (malformation). ACC is
found in many...
- "Craniocervical
junction malformation in a
child with Oromandibular-limb
hypogenesis-Möbius syndrome".
Orphanet J Rare Dis. 2: 2. doi:10.1186/1750-1172-2-2...
-
Leydig cell
hypoplasia (or aplasia) (LCH), also
known as
Leydig cell agenesis, is a rare
autosomal recessive genetic and
endocrine syndrome affecting an...
-
while three had
brain malformations including dilated ventricles with
hypogenesis of the
corpus callosum and Dandy–Walker malformation.
Trisomy 9 can be...
-
particularly limb
defects in a
syndrome known as
oromandibular limb
hypogenesis syndrome.
Hanhart Syndrome Amor DJ,
Craig JE (January 2001). "Situs inversus...
-
syndrome was more
broadly classified as
syndromes of
oromandibular and limb
hypogenesis, and
comprised a
range of
disorders that all
share hypoglossia. The name...
- heterogeneous, homogenesis, homogenetic, homogeneous, hydrogen, hypogene,
hypogenesis, hypogenic, hypogenous, monogenic, oogenesis, paragenesis, pathogen,...
- Follicle-stimulating
hormone (FSH) insensitivity, or
ovarian insensitivity to FSH in females, also
referable to as
ovarian follicle hypoplasia or granulosa...
-
addition to
agenesis of the
corpus callosum,
similar conditions are
hypogenesis (partial formation),
dysgenesis (malformation), and
hypoplasia (underdevelopment...
