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  • Title: New syndrome or severe expression of Gordon syndrome? A case report.
    Author: Courtens W, Perlmutter N, Dan B, Vamos E.
    Journal: Clin Dysmorphol; 1997 Jan; 6(1):39-44. PubMed ID: 9018417.
    Abstract:
    A boy with multiple congenital anomalies including median cleft palate, bilateral hearing loss, clino- and camptodactyly, bilateral single palmar flexion creases, severe hypotonia with kyphoscoliosis and respiratory insufficiency, failure to thrive, bilateral cryptorchidism and facial dysmorphism (epicanthus, a flat nasal bridge, a small mouth, a small nose with anteverted nostrils, low-set ears, a prominent forehead, microretrognathia) is presented. His mother has a median cleft palate, bilateral hearing loss, single palmar flexion creases, and short stature. An autosomal or X-linked dominant syndrome with more severe expression in the proband than in his mother is suggested.
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