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New syndrome of skeletal, dental and hair anomalies.
Birth Defects Orig Artic Ser. 1975; 11(2):372-9.BD

Abstract

A Brother and sister are presented with the following abnormalities: dolichocephaly with tendency toward premature closure of the sagittal suture; antimongoloid slant of the eyes with epicanthal folds, full cheeks, everted lip, multiple oral frenula, mildly high-arched palate, and microdontia with possible enamel defect; posteriorly rotated low-set pinnae with deficient cartilage; a small short thorax with pectus excavatum; unusual dermatoglyphics, and abnormal hair growth and stucture; disproportionate shortening of the fibulae and the middle and distal phalanges of the toes and fingers; and somewhat flattened epiphyses. A paternal aunt gave birth to a stillborn dwarfed male with some of the same clinical features. Although an autopsy was obtained, unfortunately no roentgenograms were made.

Authors

No affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Case Reports
Journal Article

Language

eng

PubMed ID

1227553

Citation

Sensenbrenner, J A., et al. "New Syndrome of Skeletal, Dental and Hair Anomalies." Birth Defects Original Article Series, vol. 11, no. 2, 1975, pp. 372-9.
Sensenbrenner JA, Dorst JP, Owens RP. New syndrome of skeletal, dental and hair anomalies. Birth Defects Orig Artic Ser. 1975;11(2):372-9.
Sensenbrenner, J. A., Dorst, J. P., & Owens, R. P. (1975). New syndrome of skeletal, dental and hair anomalies. Birth Defects Original Article Series, 11(2), 372-9.
Sensenbrenner JA, Dorst JP, Owens RP. New Syndrome of Skeletal, Dental and Hair Anomalies. Birth Defects Orig Artic Ser. 1975;11(2):372-9. PubMed PMID: 1227553.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - New syndrome of skeletal, dental and hair anomalies. AU - Sensenbrenner,J A, AU - Dorst,J P, AU - Owens,R P, PY - 1975/1/1/pubmed PY - 1975/1/1/medline PY - 1975/1/1/entrez SP - 372 EP - 9 JF - Birth defects original article series JO - Birth Defects Orig Artic Ser VL - 11 IS - 2 N2 - A Brother and sister are presented with the following abnormalities: dolichocephaly with tendency toward premature closure of the sagittal suture; antimongoloid slant of the eyes with epicanthal folds, full cheeks, everted lip, multiple oral frenula, mildly high-arched palate, and microdontia with possible enamel defect; posteriorly rotated low-set pinnae with deficient cartilage; a small short thorax with pectus excavatum; unusual dermatoglyphics, and abnormal hair growth and stucture; disproportionate shortening of the fibulae and the middle and distal phalanges of the toes and fingers; and somewhat flattened epiphyses. A paternal aunt gave birth to a stillborn dwarfed male with some of the same clinical features. Although an autopsy was obtained, unfortunately no roentgenograms were made. SN - 0547-6844 UR - https://www.unboundmedicine.com/medline/citation/1227553/New_syndrome_of_skeletal_dental_and_hair_anomalies_ DB - PRIME DP - Unbound Medicine ER -