SYNDROMES	FEATURES
Parry Romberg Syndrome	Facial hemiatrophy
Vander Woude Syndrome	Pits of lower lip cleft of palate
Ascher’s Syndrome	Acquired double lip Blepharochalasis Non toxic thyroid enlargement.
Median Cleft Face Syndrome	Hypertelorism Median cleft of premaxilla, palate Cranium bifidum occultum.
Oro Facial Digital Syndrome	Cleft tongue clefting of mandibular alveolar process.
Miescher’s Syndrome	Cheilitis granulomatosa.
Melkersson-Rosenthal Syndrome	Cheilitis granulomatosa Facial paralysis Scrotal tongue
Peutz-Jeghers Syndrome	Multiple intestinal polyposis Pigmentation on face, oral cavity, and hands.
Beckwith Hypoglycemic Syndrome (Beckwith-Wiedeman Syndrome)	Macroglossia Neonatal hypoglycemia Microcephaly Fetal visceromegaly
Rubinstein-Taybi Syndrome	Talons cusp developmental retardation broad thumbs great toes delayed or incomplete descent of testes.
Klinefelter Syndrome (Trisomy 46)	Taurodontism XXY genetic constitution.
Gardner’s Syndrome	Multiple polyposis of large intestine osteomas of bone multiple sebaceous cysts impacted supernumerary teeth.
Ladd Syndrome	Lacrimal apparatus involvement with lacrimal sac inflammation Lacrimal gland aplasia Auricles are deformed Ear having a cup-shaped appearance Peg-shaped teeth Hypodontia Enamel hypoplasia Deviation of fingers medially or laterally (clinodactyly)