Rehabilitation of a child with partial unilateral cryptophthalmos and multiple congenital anomalies.

Transactions of the American Ophthalmological Society 1995 Vol.93() p. 219-40; discussion 241-4

Konrad H, Merriam JC, Jones IS

Abstract

[PURPOSE] This paper describes the surgical rehabilitation of a child with craniofacial anomalies, unilateral syndactyly, and partial unilateral cryptophthalmos associated with inferior colobomata of the iris and optic nerve and agenesis of the inferior rectus and inferior oblique muscles. The clinical presentation of cryptophthalmos is described.

[METHODS] The medical literature since the original description of cryptophthalmos in 1872 was reviewed to define patterns of inheritance and the incidence of associated anomalies.

[RESULTS] Including this patient, 149 case reports of cryptophthalmos were identified. In two families transmission from parent to child suggests dominant inheritance. None of the five dominant cases had any other anomalies, and all had bilateral complete cryptophthalmos. The incidence of cryptophthalmos in the remaining families is consistent with autosomal recessive inheritance. This group includes patients with bilateral, unilateral, and partial cryptophthalmos. Other anomalies are common, including those of the ear and nose, limbs, genitourinary system, and mouth and palate. Mortality in the perinatal period is associated with renal agenesis, laryngeal atresia, and pulmonary hypoplasia.

[CONCLUSIONS] Cryptophthalmos is a rare congenital anomaly with two patterns of inheritance.

추출된 의학 개체 (NER)

유형영어 표현한국어 / 풀이UMLS CUI출처등장
해부 iris scispacy 1
해부 bilateral scispacy 1
해부 ear scispacy 1
해부 palate scispacy 1
해부 pulmonary scispacy 1
합병증 limbs scispacy 1
합병증 laryngeal atresia scispacy 1
질환 cryptophthalmos C0311249
Cryptophthalmos
scispacy 1
질환 congenital anomalies C0000768
Congenital Abnormality
scispacy 1
질환 craniofacial anomalies C0376634
Craniofacial Abnormalities
scispacy 1
질환 inferior colobomata scispacy 1
질환 agenesis C0000846
Agenesis
scispacy 1
질환 anomalies C0000769
teratologic
scispacy 1
질환 autosomal recessive inheritance C0441748
Autosomal recessive inheritance
scispacy 1
질환 palate C0700374
Palate
scispacy 1
질환 renal agenesis C0542519
Congenital absence of kidney
scispacy 1
질환 laryngeal atresia C0265756
Congenital atresia of larynx
scispacy 1
질환 pulmonary hypoplasia C0265783
Congenital hypoplasia of lung
scispacy 1
질환 congenital anomaly C0000768
Congenital Abnormality
scispacy 1
질환 renal scispacy 1
기타 optic nerve scispacy 1

MeSH Terms

Abnormalities, Multiple; Adult; Child, Preschool; Coloboma; Eye Abnormalities; Eyelids; Face; Female; Humans; Iris; Male; Oculomotor Muscles; Optic Nerve; Orbit; Radiography; Skull; Surgery, Plastic; Syndactyly