Hypoglossia

Hypoglossia
Classification and external resources
Specialty	medical genetics
ICD-10	Q38.3

Hypoglossia is a short, incompletely developed tongue. It can occur either as an isolated malformation or in association with other deformities,^[1] particularly limb defects in a syndrome known as oromandibular limb hypogenesis syndrome.

References

↑ Amor DJ, Craig JE (January 2001). "Situs inversus totalis and congenital hypoglossia". Clin. Dysmorphol. 10 (1): 47–50. doi:10.1097/00019605-200101000-00010. PMID 11152148.

Congenital malformations and deformations of digestive system (Q35–Q45, 749–751)

Upper GI tract

Tongue, mouth and pharynx	Cleft lip and palate Van der Woude syndrome tongue Ankyloglossia Macroglossia Hypoglossia

Esophagus	EA/TEF Esophageal atresia: types A, B, C, and D Tracheoesophageal fistula: types B, C, D and E esophageal rings Esophageal web (upper) Schatzki ring (lower)

Stomach	Pyloric stenosis Hiatus hernia

Lower GI tract

Intestines	Intestinal atresia Duodenal atresia Meckel's diverticulum Hirschsprung's disease Intestinal malrotation Dolichocolon Enteric duplication cyst

Rectum/anal canal	Imperforate anus Rectovestibular fistula Persistent cloaca Rectal atresia

Accessory

Pancreas	Annular pancreas Accessory pancreas Johanson–Blizzard syndrome Pancreas divisum

Bile duct	Choledochal cysts Caroli disease Biliary atresia

Liver	Alagille syndrome Polycystic liver disease

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