Median cleft of the upper lip associated with lipomas of the central nervous system and cutaneous polyps

Author:

Pai G. S.,Levkoff Abner H.,Leithiser Richard E.,Reynolds James F.

Publisher

Wiley

Subject

Genetics (clinical)

Reference17 articles.

1. (1971): Familial holoprosencephaly. In (ed): “The Third Conference on the Clinical Delineation of Birth Defects: Part XI Orofacial Structures.” Baltimore: The National Foundation—March of Dimes and The Williams and Wilkins Company,

2. The median cleft face syndrome: Differential diagnosis of cranium bifidum occultum, hypertelorism, and median cleft nose, lip, and palate

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1. Case report: Pai syndrome with multiple ventricular septal defect and without cleft palate;Clinical Neurology and Neurosurgery;2024-01

2. Pai syndrome associated with cerebral arteriovenous malformation;Journal of Oral and Maxillofacial Surgery, Medicine, and Pathology;2023-09

3. Midline cleft of the upper lip associated with a microform unilateral cleft and a proboscis-like structure: a case report;Journal of the Korean Association of Oral and Maxillofacial Surgeons;2023-08-31

4. Oculoauriculofrontonasal syndrome: Refining the phenotype through a new case series and literature review;American Journal of Medical Genetics Part A;2023-06-07

5. Cleft 0/14;Facial Reconstruction of Unusual Facial Clefts;2023

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