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Saethre-Chotzen syndrome

Saethre-Chotzen syndrome (SCS) is an inherited craniosynostosis syndrome characterized by unilateral or bilateral coronal synostosis, facial asymmetry, ptosis, strabismus and small ears with prominent crus, among other less common manifestations.

Short finger

Abnormally short finger associated with developmental hypoplasia.

Total: 2

(per page)

PMID (PMCID)
7554354	FEMALE
	Gorlin-Chaudhry-Moss or Saethre-Chotzen syndrome?
	Preis S, Kaewel EV, Majewski F. Clin Genet. 1995;47(5):267-9.
	Since the autosomal dominant Saethre-Chotzen syndrome may show similar cranio-facial features, short fingers with non-obligatory cutaneous syndactyly, and ossification defects of the cranial vault, the Saethre-Chotzen syndrome should also be considered in our patient.
7554354	FEMALE
	Gorlin-Chaudhry-Moss or Saethre-Chotzen syndrome?
	Preis S, Kaewel EV, Majewski F. Clin Genet. 1995;47(5):267-9.
	Since the autosomal dominant Saethre-Chotzen syndrome may show similar cranio-facial features, short fingers with non-obligatory cutaneous syndactyly, and ossification defects of the cranial vault, the Saethre-Chotzen syndrome should also be considered in our patient.