Rare – Page 590 – CheckOrphan

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Robinow syndrome- autosomal recessive

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Microcephaly with normal intelligence- immunodeficiency

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Succinate coenzyme Q reductase deficiency of

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Oculocutaneous albinism type 2

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Oculocutaneous albinism type 1B

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Chromosome 1q deletion

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Oculocerebral hypopigmentation syndrome type Preus

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Oculocerebral hypopigmentation syndrome Cross type

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Oculoauriculofrontonasal syndrome

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Microcephaly with spastic quadriplegia

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