罕见的

Sebaceoma (sebaceous epithelioma) is an uncommon cutaneous adnexal tumor with differentiation toward sebaceous unit.

要皮脂瘤(皮脂腺上皮瘤)是具有皮脂腺分化特徵表皮附属器肿瘤。

He had been crippled by a rare type of paralysis spreading from his ankle.

一麻痹症从他踝部扩散开来，最终道致他残废。

It was a time when motorcars were rare.

那是汽车很时代。

The unusually hot sun has fried up the crops.

烈日烤坏了庄稼。

Chicago was blacked out yesterday after a freak flood.

芝加哥昨天因为一场洪水而全城断电。

The plastic surgeon diagnosed my illness as a rare bone disease.

整形外科医生诊断出我是一骨。

The doctor diagnosed my illness as a rare skin disease.

医生诊断我为皮肤。

Aids victims often develop a rare type of cancer.

艾滋患者往往会罹患某癌症。

Congenital self-healing reticulohistiocytosis, also known as Hashimoto-Pritzker disease) is a rare variant of Langerhans cell histiocytosis.

要先天性自愈性网状组织细胞增生症是兰格氏组织细胞增生症中一型态。

Milagros was born with a rare congenital condition called sirenomelia, which is also known as "mermaid syndrome".

塞隆出生时就患有一先天性疾“并腿畸形”，又被称为“美人鱼综合徵”。

Adverse effects associated with short-term gonadorelin agonists are common, but are rarely serious enough to require drug withdrawal.

短期促性腺激素释放因子治疗相关副作用是常，但严重到足以停药程度是。

To report two cases of rare primary lacrimal sac tumor-one of inverted papilloma and the other of hemangiopericytoma.

提出两例上皮性和非上皮性泪囊肿瘤报告。

Incontinentia pigmenti is a rare genodermatosis that usually affects female infants.The associated abnormalities involve ocular, dental, skeletal and central nervous systems.

色素失禁症是一皮肤遗传疾，通常发生在女性，除了皮肤以外还可能出现眼睛，牙齿，骨骼，以及中枢神经系统异常。

Orbital meningocele is a rare congenital anomaly with cystic herniation of meninges caused by a bony defect of the cranio-orbital bone.

要眼窝脑膜膨出是先天性异常，其成因为头颅或眼窝骨缺损使得脑脑从缺损处呈囊状膨出。

Hay-Wells Syndrome (HWS), also known as the ankyloblepharon-ectodermal dysplasia-clefting (AEC) syndrome, is one of at least 150 known types of ectodermal dysplasia.

什麽是'海伊井综合徵-先天性条件影响皮肤头发和指甲'?

Galactosemia is another rare metabolic disorder that occurs when the liver enzyme GALT, needed to break down galactose, is partially or completely absent.

半乳糖血症是另一代谢功能紊乱疾，因为缺乏分解半乳糖酶（高尔特？）所致。

Dehiscence of the floor of the hypotympanum with protrusion of the jugular bulb into the middle ear cavity is a rare otological finding.

要颈静脉球经下鼓室底部骨层裂隙膨入中耳腔，是一中耳腔血管异常。

Systemic mastocytosis results in the accumulation of mast cells in various tissues.We report a rare case of systemic mastocytosis presenting with cholestatic liver disease.

系统性肥大导致肥大细胞在各组织中集聚，我们报告一例系统性肥大症与胆汁淤积性肝。

Macrodactyly is a rare congenital malformation characterized by an increase in the size of all the elements or structures of a digit or digits.

要巨趾（指）症是相当一先天性脚趾（手指）过度增生一畸形，严重者脚蹠（手掌）也会肥厚。

This paper is reported a rare case of palmoplanter keratoma hereditaria-keratoma hereditaria mutilans and differential diagnosis with various palmoplantar keratodermas and dactylolysis are discussed.

本文报告了一例遗传性掌跖皮肤角化—遗传性残毁性角化瘤,并与各掌跖皮肤角化症、断肢症鉴别进行了讨论。