Volume 80, Issue 4 pp. 303-308
Research Article
Full Access

Long first metacarpal in monozygotic twins with probable Baller-Gerold syndrome

Piergiorgio Franceschini

Corresponding Author

Piergiorgio Franceschini

Dipartimento di Scienze Pediatriche e dell'Adolescenza, Servizio di Genetica Clinica, Università di Torino, Turin, Italy

Dipartimento di Scienze Pediatriche e dell'Adolescenza, Servizio di Genetica Clinica, Università di Torino, Piazza Polonia 94, I-10126, Torino, Italia.Search for more papers by this author
Domenico Licata

Domenico Licata

Dipartimento di Scienze Pediatriche e dell'Adolescenza, Servizio di Genetica Clinica, Università di Torino, Turin, Italy

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Andrea Guala

Andrea Guala

Dipartimento di Scienze Pediatriche e dell'Adolescenza, Servizio di Genetica Clinica, Università di Torino, Turin, Italy

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Giuseppe Di Cara

Giuseppe Di Cara

Dipartimento di Scienze Pediatriche e dell'Adolescenza, Servizio di Genetica Clinica, Università di Torino, Turin, Italy

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Federico Signorile

Federico Signorile

Dipartimento di Scienze Pediatriche e dell'Adolescenza, Servizio di Genetica Clinica, Università di Torino, Turin, Italy

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Daniele Franceschini

Daniele Franceschini

I Clinica Ortopedica, Università di Torino, Turin, Italy

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Lorenzo Genitori

Lorenzo Genitori

O.I.R.M.-S. Anna, Servizio di Neurochirurgia Pediatrica, Turin, Italy

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Gabriella Restagno

Gabriella Restagno

Dipartimento di Patologia Clinica, Settore Genetica Molecolare, Turin, Italy

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Abstract

We report on a pair of monozygotic twins with probable Baller-Gerold syndrome (BGS). Twin A had severe coronal craniosynostosis. Twin B had right radioulnar and ipsilateral first metacarpal hypoplasia. Both had bilateral fifth finger clinodactyly. Assuming that the twins were truly monozygotic, a single genetic disorder (i.e., BGS) could explain the variable expression. Together the twins have the typical anomalies of BGS. The diagnosis was supported by the metacarpophalangeal profile (MPP) which confirmed hypoplasia of the first right metacarpal in Twin A and bilateral fifth finger brachymesophalangy in both twins. Furthermore, the MPP showed an unexpected abnormal lengthening of the first metacarpal (unilateral in Twin A and bilateral in Twin B), a previously undetected radial ray defect in BGS. These findings suggest the possibility that the MPP may assist recognition of mild cases of BGS such as those with apparently isolated craniosynostosis or isolated upper limbs defects. Am. J. Med. Genet. 80:303–308, 1998. © 1998 Wiley-Liss, Inc.

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