The Chamber Angle in Split-Pupil

Absence of PITX2, BARX1, and FOXC1 mutations in De Hauwere syndrome (Axenfeld–Rieger anomaly, hydrocephaly, hearing loss): A 25‐year follow up

“…Our patient fulfils the criteria proposed by De Hauwere et al [1973] with the difference that she is of normal intelligence. Von Noorden and Baller [1963] patient had features consistent with this syndrome including Axenfeld–Rieger eye anomaly, hydrocephalus, and psychomotor retardation in a 14‐month‐old boy. He also had cerebellar hypoplasia.…”

“…They described a mother and three affected children. Von Noorden and Baller [1963] reported a probable case. Chitty et al [1991] and Van Daele et al [1996] documented patients with some overlapping features but whose major component was partially absent or fibrotic eye muscles.…”

Absence of PITX2, BARX1, and FOXC1 mutations in De Hauwere syndrome (Axenfeld–Rieger anomaly, hydrocephaly, hearing loss): A 25‐year follow up

“…Our patient fulfils the criteria proposed by De Hauwere et al [1973] with the difference that she is of normal intelligence. Von Noorden and Baller [1963] patient had features consistent with this syndrome including Axenfeld–Rieger eye anomaly, hydrocephalus, and psychomotor retardation in a 14‐month‐old boy. He also had cerebellar hypoplasia.…”

“…They described a mother and three affected children. Von Noorden and Baller [1963] reported a probable case. Chitty et al [1991] and Van Daele et al [1996] documented patients with some overlapping features but whose major component was partially absent or fibrotic eye muscles.…”

Absence of PITX2, BARX1, and FOXC1 mutations in De Hauwere syndrome (Axenfeld–Rieger anomaly, hydrocephaly, hearing loss): A 25‐year follow up

“…Our patient fulfils the criteria proposed by De Hauwere et al [1973] with the difference that she is of normal intelligence. Von Noorden and Baller [1963] patient had features consistent with this syndrome including Axenfeld–Rieger eye anomaly, hydrocephalus, and psychomotor retardation in a 14‐month‐old boy. He also had cerebellar hypoplasia.…”

“…They described a mother and three affected children. Von Noorden and Baller [1963] reported a probable case. Chitty et al [1991] and Van Daele et al [1996] documented patients with some overlapping features but whose major component was partially absent or fibrotic eye muscles.…”

Absence of PITX2, BARX1, and FOXC1 mutations in De Hauwere syndrome (Axenfeld–Rieger anomaly, hydrocephaly, hearing loss): A 25‐year follow up

“…Our patient fulfils the criteria proposed by De Hauwere et al [1973] with the difference that she is of normal intelligence. Von Noorden and Baller [1963] patient had features consistent with this syndrome including Axenfeld–Rieger eye anomaly, hydrocephalus, and psychomotor retardation in a 14‐month‐old boy. He also had cerebellar hypoplasia.…”

“…They described a mother and three affected children. Von Noorden and Baller [1963] reported a probable case. Chitty et al [1991] and Van Daele et al [1996] documented patients with some overlapping features but whose major component was partially absent or fibrotic eye muscles.…”