Carey-Fineman-Ziter syndrome: a report of a new patient and phenotype delineation (CROSBI ID 502156)
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Podaci o odgovornosti
Barišić, Ingeborg ; Petković, Giorgie
engleski
Carey-Fineman-Ziter syndrome: a report of a new patient and phenotype delineation
Carey-Fineman-Ziter syndrome is a very rare disorder characterized by a dysmorphic face, Moebius and Robin sequences, congenital myopathy, and growth retardation. Skeletal anomalies and developmental delay are occasionaly present. Only 6 patients have been described so far, two sporadic cases and two pairs of siblings suggesting autosomal recessive inheritance. We report a 9-year old girl with remarkably similar anomalies. Her unusual facial features included high forehead, prominent metopic suture, antimongoloid eye slanting, strabism, high myopia, low-set, poorly shaped ears, hypoplastic alae nasi, short philtrum, cupid shaped, short upper lip, small mouth with receding angles, and Robin sequence. She also had Moebius sequence resulting in distinct functional abnormalities involving eye movement, facial expression, mouth closure, speech and swallowing. During early infancy difficulties in sucking, failure to thrive and marked hypotonia were noted. Shehad bilateral talipes equinovarus with hyperlaxity of other joints. Neurological evaluation showed multiple lesions of the cranial nerves, predominantly n. abducens, and bilateral facial nerve palsy, striking atrophy of the lower leg muscles, reduced deep-tendon reflexes and signs of lower motor neuron lesion on EMG which have not been observed in reported patients so far. Her mental development was within the normal range, although motor defecit, slow speech development, short attentiion span, hyperactivity and disturbances of visual and motor organisation and integration were noted. Our patient delineates the features of Carey-Fineman-Ziter syndrome confirming the Moebius-Robin Sequence associatin to congenital neuromuscular disorders.
Carey-Fineman-Ziter syndrome; Mobius sequence; Robin sequence; congenital myopathy
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Podaci o prilogu
125-125-x.
2004.
objavljeno
Podaci o matičnoj publikaciji
European Journal of Human Genetics (1018-4813) 12 (2004), suppl 1 ; 125
van Ommen, Gert-Jan B.
London : Delhi: Nature publishing group
Podaci o skupu
European Human Genetics Conference 2004
poster
12.06.2004-15.06.2004
München, Njemačka