20p12.3 deletion is rare cause of syndromic cleft palate: case report and review of literature
The proband was referred for chromosome analysis when he was 5 years old because of
psychomotor delay and unusual facies. He was the latest child of unrelated, healthy
parents. The father was 38 and the mother 28 at the time of his birth. He was born
after an uncomplicated 39Â weeks pregnancy, and normal vaginal delivery. As a newborn
the patient had a short period of cyanosis, and showed congenital hypotonia. Weight
was 2100Â g (3rd centile), length 45Â cm (3rd centile), head circumference 34Â cm (30th
centile). In subsequent evaluation, he showed a failure to thrive and slight delay
in the acquisitions of motor milestones; the patient was able to sit with 12Â months,
and could walk of 2 years, first words were spoken at 36Â months, nevertheless, he
still retains language disorders and early intervention speech-language therapy was
initiated. Length, weight and head circumference at 5 years were 99Â cm (3rd centile),
16Â kg (15th), and 50Â cm (40th centile), respectively. He had submucous CP with bifid
uvula, small forehead, hypertelorism and downslanting palpebral fissures. The nasal
bridge was broad and the nasal tip was bulbous. He had low set ears, short philtrum,
down turned corners of the mouth and micrognathia. The remaining physical examination
was notable for widespread tooth decay and dental overlapping. There were no significant
limb anomalies, or cardiovascular disorders. CT scan of the brain was normal, electroencephalogram
showed no paroxysmal abnormalities. Ophthalmologic examination and thyroid functions
were normal. X-ray examination showed that his bone age was 2 years. Family history
revealed an older brother with bilateral cleft lip, but further details were not available.
Cytogenetic and molecular cytogenetic analysis
Cytogenetic analysis was carried out on the patient and his parents. The study included
peripheral lymphocyte culture by a standard method using a reverse banding technique
(RHG banding), and G-banding technique using trypsin. About 0.4–0.8 mL of peripheral
blood was incubated in complete lymphocyte culture medium for 72Â h. Metaphases were
harvested by adding karyomax colcemid solution for 50Â min followed by hypotonic KCl
(0.075Â M) treatment for 20Â min and fixation using standard 3:1 methanol and acetic
acid fixative 5]. At least 11 metaphases were scored. A high-resolution analysis was done by synchronization
using thymidine solution (15 mg/mL) for 16 h before harvesting 5]. Fluorescence in situ hybridization (FISH) was performed on patient’s metaphases
obtained from whole blood cultures. Subsequent probes were applied on lymphocyte metaphase
spreads prepared from the propositus: centromere 20 specific probe (D20Z1 in 20q11.1,
Abbott/Vysis, Wiesbaden, Germany), whole chromosome paint for chromosome 20 (homemade
WCP), bacterial artificial chromosome (BAC) clones; RP11-96L6 in 20p11.21, and RP11-116E13
in 20p12.3 6].