This was a very challenging case, and there was not a good way that I found to approach it. The authors had the benefit of having the radiological diagnosis of the mother, but let us see what we could do without the knowledge of the maternal condition.
Findings
There were a variety of findings (the prominent supraorbital ridge, the clenched fist, the sandal gap, a narrow chest). The baby and mom pictures were notable for the coarse facial features and the prominent supraorbital ridge again. The X-ray demonstrated flaring of the metaphysis.
Approach to the diagnosis
Of all these finding the most unusual was the "prominent supraorbital ridgeâ€. However this was not a very useful criterion in the search. Those keywords gave no match with OMIM and in Medline, only one article (Whistling face syndrome) came up. The whistling face syndrome has many of the findings of the current syndrome but lacks the metaphyseal anomalies.
So I returned to pre-computerized information and in the Smith's book there is a section on prominent supraorbital ridge which includes several 11 conditions of which the following were quite similar to the findings:
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Borjeson-Forsman-Lehmann syndrome *
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Coffin-Lowry syndrome
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Frontometaphyseal dysplasia *
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Langer-Giedion syndrome
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Metaphyseal chondrodysplasia *
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Oto-palato-digital syndrome *
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Pyle metaphyseal dysplasia *
Another differential diagnosis was Freeman Sheldon syndrome.
I am not really sure that I could have gone past these. Interestingly searching OMIM on "prominent brow" did not provide any further information but "prominent supraciliary ridge" immediately suggested frontometaphyseal dysplasia, which was the final diagnosis.