N = Chromosomal Abnormalities |
Cri-du-Chat(5P-) Syndrome
Moonshaped face,
with microcephaly,hypertelorism, epicanthal folds,
antimongoloid slant,flaccid epiglottis,abnormal
phonation. Hypoplasia of larynx causes catlike cry
(cri-du-chat), low-set ears and preauricular tags.
Chromosomal abnormality shows terminal deletion
of short arm of one chromosome 5
(Deleted segment 5P14 - 5P ter)
N1 = Abnormality in
1P+
N2 = Abnormality in 1P-
N3 = Abnormality in 1Q+
N4 = Abnormality in 1Q-
N5 = Abnormality in 2P+
N6 = Abnormality in 2P-
N7 = Abnormality in 2Q+
N8 = Abnormality in 2Q-
N9 = Abnormality in 3P+
N10 = Abnormality in 3P-
N11 = Abnormality in 3Q+
N12 = Abnormality in 3Q-
N13 = Abnormality in 4P+
N14 = Abnormality in 4P-
(
Wolf 's syndrome )
N15 = Abnormality in 4Q+
N16 = Abnormality in 4Q-
N17 = Abnormality in 5P+
N18 = Abnormality in 5P-
( Cri du Chat syndrome )
N19 = Abnormality in 5Q+
N20 = Abnormality in 5Q-
N21 = Abnormality in 6P+
N22 = Abnormality in 6P-
N23 = Abnormality in 6Q+
N24 = Abnormality in 6Q-
N25 = Abnormality in 7P+
N26 = Abnormality in 7P-
N27 = Abnormality in 7Q+
N28 = Abnormality in 7Q-
N29 = Abnormality in 8P+
N30 = Abnormality in 8P-
N31 = Abnormality in 8Q+
N32 = Abnormality in 8Q-
N33 = Abnormality in 8+ (Trisomy
8)
N34 = Abnormality in 9P+
N35 = Abnormality in 9P-
________________
Back Next
To Author: |
Dr.Jarind B. Sriraumpuch |
Home |
Page=g_listn1 |
Update since
10/09/50