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June 1966, Vol 111, No. 6 >
Article | June 1966

Picture of the Month FREE

SYDNEY S. GELLIS, MD; MURRAY FEINGOLD, MD
Am J Dis Child. 1966;111(6):635-636. doi:10.1001/archpedi.1966.02090090107010.
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Denouement and Discussion 

HALLERMANN-STREIFF SYNDROME  (Dyscephalia Mandibulo-Oculo-Facialis, Dyscephalia of François)

MANIFESTATIONS  The head has an abnormal shape, usually brachycephalic or scaphocephalic. The frontal and parietal bones may be enlarged, and the fontanels remain open. The cranial vault appears enlarged in proportion to the small face. The nose is usually thin and beaked, with a sharp nasofrontal angle. There is striking micrognathia, and the mouth is small with thin lips and a high-arched palate. There are various dental abnormalities ranging from fully erupted teeth at birth to numerous malformed or absent teeth. Occasionally, there is limitation of opening of the mouth due to deformities of the temporomandibular joint. The ears are frequently low set; however, hearing

REFERENCES

1 +
Streiff, E.B.:  Dysmorphie Mandibulo-Faciale et Alterations Oculaires , Ophthalmologica 120:79-83, 1950;.
2 +
François, J.:  A New Syndrome , Arch Ophthal 60:842-862, 1958;.
3 +
Hoefnagel, D., and Benirschke, K.:  Dyscephalia Mandibulo-Oculo-Facialis , Arch Dis Child 40:57-61, 1965;.

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Country-Specific Mortality and Growth Failure in Infancy and Yound Children and Association With Material Stature

Use interactive graphics and maps to view and sort country-specific infant and early dhildhood mortality and growth failure data and their association with maternal

References

1 +
Streiff, E.B.:  Dysmorphie Mandibulo-Faciale et Alterations Oculaires , Ophthalmologica 120:79-83, 1950;.
2 +
François, J.:  A New Syndrome , Arch Ophthal 60:842-862, 1958;.
3 +
Hoefnagel, D., and Benirschke, K.:  Dyscephalia Mandibulo-Oculo-Facialis , Arch Dis Child 40:57-61, 1965;.

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