- scan
proposed that the
chromosomal locus of
camptodactyly was 3q11.2-q13.12. The
specific cause of
camptodactyly remains unknown, but
there are a few deficiencies...
- an
incline between 15° and 30° is typical. A similar-sounding term,
camptodactyly, is a
fixed flexion deformity of a digit.[citation needed] Treatment...
-
Camptodactyly-taurinuria syndrome, also
known as
familial streblodactyly with
amino aciduria is a very rare
autosomal dominant genetic disorder which...
- deep-set nails, thin hair,
short ribs,
limited elbow and knee extension,
camptodactyly, and a co****, low-pitched voice. Dela****
development of
motor skills...
- multi-systemic
genetic disorder which is
characterized by the
presence of
camptodactyly,
flattened vertebrae and
thoracic scoliosis of
varying degrees. It has...
- Lenz
microphthalmia syndrome is a very rare
inherited disorder characterized by
abnormal smallness of one or both eyes (microphthalmos)
sometimes with...
-
Camptodactyly, tall stature, and
hearing loss syndrome, also
known as
CATSHL syndrome, is a rare
genetic disorder which consists of
camptodactyly, tall...
- dwarfism-cleft palate-
camptodactyly is a rare
genetic disorder which is
characterized by
mesomelic limb
shortening and bowing,
finger camptodactyly, skin dimpling...
- Tel
Hashomer camptodactyly syndrome is a rare
genetic disorder which is
characterized by
camptodactyly,( a
condition where one or more
fingers or toes...
-
Gordon syndrome Other names Camptodactyly-cleft palate-clubfoot
syndrome Gordon syndrome is
inherited in an
autosomal dominant manner...
