H. Kawame et al., DIGITAL ANOMALIES, MICROCEPHALY, AND NORMAL INTELLIGENCE - NEW SYNDROME OR FEINGOLD SYNDROME, American journal of medical genetics, 69(3), 1997, pp. 240-244
We present four patients-two boys and their mother and an unrelated gi
rl-with microcephaly, normal intelligence, and distal abnormalities, T
he hand abnormalities are characterized by brachydactyly with radial c
linodactyly of the fourth and fifth fingers, ulnar clinodactyly of the
second fingers, and an increased space between the second and third f
ingers associated with an abnormal palmar crease that extends to the u
lnar border, The foot abnormalities include short toes with syndactyly
of the fourth and fifth toes, The mother has normal intelligence, and
her sons and the unrelated girl have normal development, Although sim
ilar digital abnormalities, microcephaly, and normal intelligence were
described by Feingold in patients with gastrointestinal atresia, we t
hink that our patients' findings represent a different condition, The
most likely mode of inheritance is autosomal dominant, The clinical re
cognition of this syndrome will allow for appropriate genetic counseli
ng as well as provision of information on natural history, i.e., norma
l intelligence. (C) 1997 Wiley-Liss, Inc.