In most cases, anomalies including hypertelorism, epicantus, upward-slanting palpebral fissures, clinodactyly
in the fifth finger, short nail folds, pes planus, joint laxity, dental problems and radioulnar synostosis have been identified (4, 7).
Additionally there was medial inclination of index finger and clinodactyly
of 5th finger.
The respiratory and heart rates were 80/min and 160/min respectively, The patient had a flat midface, widely set eyes, mild ptosis, short philtrum and a triangular mouth; polythelia, foot and hand anomalies with clinodactyly
were also noted (Fig.
There was frontal and parietal bossing, open anterior fontanelle, hypertelorism, depressed nasal bridge, high arched palate, supernumerary teeth, and clinodactyly
The digital manifestations are brachydactyly, polydactyly, syndactyly, clinodactyly
and duplicated hallux.
The most frequent hand anomaly was Kirner deformity and clinodactyly
with an incidence of 0.
is almost invariably present, resulting from the side-to-side variations in the accelerated rate of growth (3).
Because of the asymmetry of these tendon insertions, the clinical manifestation of this injury in the young mimics a mallet finger and a clinodactyly
Classic phenotypic findings include brachycephaly, epicanthal folds, palpebral fissures, macroglossia, neck skinfolds, clinodactyly
, single transverse palmar creases, and widely spaced first and second toes (Nehring, 2010).
Furthermore, variable anomalies of the hands and feet, such as duplicated terminal phalanx of the thumb, triphalangeal thumb (long finger-like thumb with three phalanges instead of two), preaxial polydactyly (thumb duplication), syndactyly (fusion) of the second and third digits, and fifth finger clinodactyly
(curving of the fifth finger towards the fourth) have also be seen in cases with LADD [Guven et al.
The patient was a 2-month-old girl with multiple congenital abnormalities including cleft lip and palate, hypertelorism, malformed ears, clinodactyly
and ulnar deviation of the hands, abdominal wall defect (omphalocele), malpositioned anus and cardiac defect (ventircular septal defect).
YK 9 / M right-sided 6 -- undescended testis pallor, bruising" hepatomegaly (4 cm) splenomegaly (5 cm) cafe-au-lait spots ear abnormalities clinodactyly
Notable physical exam features include widely spaced eyes (hypertelorism), bulbous nasal tip, high arched palate, and fifth finger clinodactyly
These individuals have features like micrognathia, hypertelorism, high arched palate, cleft palate, clinodactyly
and short stature.
Second trimester ultrasound markers for trisomy 21 include: Brachycephaly, mild ventriculomegaly, nuchal oedema (or nuchal fold thickness), nasal hypoplasia, cardiac defects (manily atrioventricular septal defects), duodenal atresia and echogenic bowel, mild hydronephrosis, shortening of both the femur and more so, the humerus, sandal gap and clinodactyly
or midphylanx hypoplasia of the fifth finger.