10042 |
c.16C > G |
p.Leu6Val |
Paternal |
SHH, SIX3, ZIC2 and TGIF are normal |
Lobar HPE, hypotelorism, single nostril, cleft lip/palate. Father is phenotypically unaffected, mother described as having clear “microforms” of HPE |
This study |
9490 |
c.133C > G |
p.Arg45Gly |
Paternal |
de novo ZIC2: c.994_1005dup, p. Cys335_Pro338dup; SHH, SIX3, TGIF are normal |
Semilobar HPE, developmental delay, agenesis of the corpus callosum, microcephaly and spasticity |
This study |
Patient 1 |
c.599C > G |
p.Thr200Arg |
NA |
SHH, SIX3, ZIC2 and TGIF are normal |
Semilobar HPE, developmental delay, hypoplastic midface, upslanting palpebral fissures, proptosis, depressed nasal bridge, absent collumella, and bilateral cleft lip and palate |
Ribeiro et al. (2010) |
1024 |
c.660C > G |
p.Asn220Lys |
Paternal |
ZIC2: c.709_711dup; p.His239dup (polymorphism); SHH, SIX3 and TGIF are normal |
Hypoplastic corpus callosum, diabetes insipidus, craniosynostosis of metopic suture, pyriform apeture stenosis, midline cleft lip with complete premaxillary agenesis |
This study |
Patient 7 |
c.736G > T |
p.Ala246Ser |
NA |
No data available |
No data available |
Ribeiro et al. (2010) |
Patient 2 |
c.775G > A |
p.Gly259Arg |
NA |
Normal karyotype, SHH, SIX3, TGIF, ZIC2 and GLI2 are normal |
Hypotelorism, with proptosis, hypoplastic midface, depressed nasal bridge, absent collumella with notching of the tip, bilateral cleft lip and palate |
Ribeiro et al. (2010) |
Patient 3 |
c.808G > T |
p.Asp270Tyr |
NA |
Paternally inherited SHH: c.653T > C, p.Leu218Pro; SIX3, ZIC2, TGIF and GLI2 are normal |
Microcephaly, hypotelorism, hypoplastic midface, depressed nasal bridge and nasal bones, right cleft lip and palate, no brain structural anomalies |
Ribeiro et al. (2010) |
Patient 4 |
c.863A > G |
p.Asp288Gly |
de novo |
de novo SHH: c.1088G > A, p.Cys363Tyr |
Microcephaly, hypotelorism, midface hypoplasia, hypoplastic nasal bones, depressed nasal bridge, midline cleft lip and palate |
Ribeiro et al. (2010) |
6386 |
c.928C > T |
p.Pro310Ser |
Paternal |
SHH, SIX3, ZIC2 and TGIF are normal |
Semilobar HPE, absent pituitary and olfactory bulbs, microcephaly, hypotelorism, midface hypoplasia, depressed nasal bridge and hypoplastic septum, midline cleft lip with intact palate, micropenis |
This study |
4953 |
c.958G > T |
p.Gly320Cys |
Mother is normal; father is unavailable |
ZIC2: c.709_711dup; p.His239dup (polymorphism); SHH, SIX3 and TGIF: are normal |
HPE, no further clinical data available |
This study |